Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(Thalassemia). Showing records 1 – 30 of 172 total matches.

[1] [2] [3] [4] [5] [6]

Search Limiters

Last 2 Years | English Only

Degrees

Levels

Languages

Country

▼ Search Limiters


University of Hong Kong

1. 何廣慧; Ho, Sophia KW. Detection of clinically silent alpha-globin gene mutations in Chinese using high resolution melting analysis.

Degree: Master of Medical Sciences, 2014, University of Hong Kong

α-thalassemia is an inherited globin gene disorder commonly found among the Chinese population. It is composed of both non-deletional and deletional α-globin gene mutations. Classical… (more)

Subjects/Keywords: Thalassemia - Diagnosis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

何廣慧; Ho, S. K. (2014). Detection of clinically silent alpha-globin gene mutations in Chinese using high resolution melting analysis. (Masters Thesis). University of Hong Kong. Retrieved from Ho, S. K. W. [何廣慧]. (2014). Detection of clinically silent alpha-globin gene mutations in Chinese using high resolution melting analysis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5318929 ; http://dx.doi.org/10.5353/th_b5318929 ; http://hdl.handle.net/10722/206558

Chicago Manual of Style (16th Edition):

何廣慧; Ho, Sophia KW. “Detection of clinically silent alpha-globin gene mutations in Chinese using high resolution melting analysis.” 2014. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. Ho, S. K. W. [何廣慧]. (2014). Detection of clinically silent alpha-globin gene mutations in Chinese using high resolution melting analysis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5318929 ; http://dx.doi.org/10.5353/th_b5318929 ; http://hdl.handle.net/10722/206558.

MLA Handbook (7th Edition):

何廣慧; Ho, Sophia KW. “Detection of clinically silent alpha-globin gene mutations in Chinese using high resolution melting analysis.” 2014. Web. 28 Mar 2020.

Vancouver:

何廣慧; Ho SK. Detection of clinically silent alpha-globin gene mutations in Chinese using high resolution melting analysis. [Internet] [Masters thesis]. University of Hong Kong; 2014. [cited 2020 Mar 28]. Available from: Ho, S. K. W. [何廣慧]. (2014). Detection of clinically silent alpha-globin gene mutations in Chinese using high resolution melting analysis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5318929 ; http://dx.doi.org/10.5353/th_b5318929 ; http://hdl.handle.net/10722/206558.

Council of Science Editors:

何廣慧; Ho SK. Detection of clinically silent alpha-globin gene mutations in Chinese using high resolution melting analysis. [Masters Thesis]. University of Hong Kong; 2014. Available from: Ho, S. K. W. [何廣慧]. (2014). Detection of clinically silent alpha-globin gene mutations in Chinese using high resolution melting analysis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5318929 ; http://dx.doi.org/10.5353/th_b5318929 ; http://hdl.handle.net/10722/206558


Central Connecticut State University

2. Wilson, Lauren E., 1980-. The development of highly sensitive ethnicity based screening panels for β-thalassemia; The development of highly sensitive ethnicity based screening panels for β-thalassemia.

Degree: Department of Biomolecular Sciences, 2011, Central Connecticut State University

β-thalassemia is a common inherited hemoglobin disorder which results in the unbalanced synthesis of beta globin chains (2). It is an autosomal recessive disorder which… (more)

Subjects/Keywords: Thalassemia – Genetic aspects.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Wilson, Lauren E., 1. (2011). The development of highly sensitive ethnicity based screening panels for β-thalassemia; The development of highly sensitive ethnicity based screening panels for β-thalassemia. (Thesis). Central Connecticut State University. Retrieved from http://content.library.ccsu.edu/u?/ccsutheses,2316

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wilson, Lauren E., 1980-. “The development of highly sensitive ethnicity based screening panels for β-thalassemia; The development of highly sensitive ethnicity based screening panels for β-thalassemia.” 2011. Thesis, Central Connecticut State University. Accessed March 28, 2020. http://content.library.ccsu.edu/u?/ccsutheses,2316.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wilson, Lauren E., 1980-. “The development of highly sensitive ethnicity based screening panels for β-thalassemia; The development of highly sensitive ethnicity based screening panels for β-thalassemia.” 2011. Web. 28 Mar 2020.

Vancouver:

Wilson, Lauren E. 1. The development of highly sensitive ethnicity based screening panels for β-thalassemia; The development of highly sensitive ethnicity based screening panels for β-thalassemia. [Internet] [Thesis]. Central Connecticut State University; 2011. [cited 2020 Mar 28]. Available from: http://content.library.ccsu.edu/u?/ccsutheses,2316.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wilson, Lauren E. 1. The development of highly sensitive ethnicity based screening panels for β-thalassemia; The development of highly sensitive ethnicity based screening panels for β-thalassemia. [Thesis]. Central Connecticut State University; 2011. Available from: http://content.library.ccsu.edu/u?/ccsutheses,2316

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Hawaii – Manoa

3. Titus, Elizabeth Anne Brumbaugh. Characterization of embryonic globin gene expansions in homo sapiens : mechanistic and evolutionary implications.

Degree: PhD, 2009, University of Hawaii – Manoa

Microfiche.

xiii, 138 leaves, bound ill. 29 cm

This research focused on the characterization of aberrant ζ-globin expansions as an important model system in the… (more)

Subjects/Keywords: Globin genes; Hemoglobin polymorphisms; Thalassemia

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Titus, E. A. B. (2009). Characterization of embryonic globin gene expansions in homo sapiens : mechanistic and evolutionary implications. (Doctoral Dissertation). University of Hawaii – Manoa. Retrieved from http://hdl.handle.net/10125/9398

Chicago Manual of Style (16th Edition):

Titus, Elizabeth Anne Brumbaugh. “Characterization of embryonic globin gene expansions in homo sapiens : mechanistic and evolutionary implications.” 2009. Doctoral Dissertation, University of Hawaii – Manoa. Accessed March 28, 2020. http://hdl.handle.net/10125/9398.

MLA Handbook (7th Edition):

Titus, Elizabeth Anne Brumbaugh. “Characterization of embryonic globin gene expansions in homo sapiens : mechanistic and evolutionary implications.” 2009. Web. 28 Mar 2020.

Vancouver:

Titus EAB. Characterization of embryonic globin gene expansions in homo sapiens : mechanistic and evolutionary implications. [Internet] [Doctoral dissertation]. University of Hawaii – Manoa; 2009. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10125/9398.

Council of Science Editors:

Titus EAB. Characterization of embryonic globin gene expansions in homo sapiens : mechanistic and evolutionary implications. [Doctoral Dissertation]. University of Hawaii – Manoa; 2009. Available from: http://hdl.handle.net/10125/9398


University of Hong Kong

4. 方乃聰; Fong, Nai-chung. Real time three dimensional echocardiographic assessment on patients with beta-thalassaemia major.

Degree: Master of Medical Sciences, 2001, University of Hong Kong

published_or_final_version

Medical Sciences

Master

Master of Medical Sciences

Subjects/Keywords: Thalassemia.; Echocardiography.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

方乃聰; Fong, N. (2001). Real time three dimensional echocardiographic assessment on patients with beta-thalassaemia major. (Masters Thesis). University of Hong Kong. Retrieved from Fong, N. [方乃聰]. (2001). Real time three dimensional echocardiographic assessment on patients with beta-thalassaemia major. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3197024 ; http://dx.doi.org/10.5353/th_b3197024 ; http://hdl.handle.net/10722/29712

Chicago Manual of Style (16th Edition):

方乃聰; Fong, Nai-chung. “Real time three dimensional echocardiographic assessment on patients with beta-thalassaemia major.” 2001. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. Fong, N. [方乃聰]. (2001). Real time three dimensional echocardiographic assessment on patients with beta-thalassaemia major. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3197024 ; http://dx.doi.org/10.5353/th_b3197024 ; http://hdl.handle.net/10722/29712.

MLA Handbook (7th Edition):

方乃聰; Fong, Nai-chung. “Real time three dimensional echocardiographic assessment on patients with beta-thalassaemia major.” 2001. Web. 28 Mar 2020.

Vancouver:

方乃聰; Fong N. Real time three dimensional echocardiographic assessment on patients with beta-thalassaemia major. [Internet] [Masters thesis]. University of Hong Kong; 2001. [cited 2020 Mar 28]. Available from: Fong, N. [方乃聰]. (2001). Real time three dimensional echocardiographic assessment on patients with beta-thalassaemia major. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3197024 ; http://dx.doi.org/10.5353/th_b3197024 ; http://hdl.handle.net/10722/29712.

Council of Science Editors:

方乃聰; Fong N. Real time three dimensional echocardiographic assessment on patients with beta-thalassaemia major. [Masters Thesis]. University of Hong Kong; 2001. Available from: Fong, N. [方乃聰]. (2001). Real time three dimensional echocardiographic assessment on patients with beta-thalassaemia major. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3197024 ; http://dx.doi.org/10.5353/th_b3197024 ; http://hdl.handle.net/10722/29712


University of Hong Kong

5. 倪艷茹; Ngai, Yim-yu. Assessing alpha globin gene amplification and its modification of beta thalassemia phenotype.

Degree: Master of Medical Sciences, 2015, University of Hong Kong

Thalassemia is the most common inherited disorder in the world. The high degree of homologous sequences on the α2 and α1 genes leads to unequal… (more)

Subjects/Keywords: Thalassemia - Genetic aspects; Globin genes

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

倪艷茹; Ngai, Y. (2015). Assessing alpha globin gene amplification and its modification of beta thalassemia phenotype. (Masters Thesis). University of Hong Kong. Retrieved from Ngai, Y. [倪艷茹]. (2015). Assessing alpha globin gene amplification and its modification of beta thalassemia phenotype. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5659400 ; http://hdl.handle.net/10722/221500

Chicago Manual of Style (16th Edition):

倪艷茹; Ngai, Yim-yu. “Assessing alpha globin gene amplification and its modification of beta thalassemia phenotype.” 2015. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. Ngai, Y. [倪艷茹]. (2015). Assessing alpha globin gene amplification and its modification of beta thalassemia phenotype. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5659400 ; http://hdl.handle.net/10722/221500.

MLA Handbook (7th Edition):

倪艷茹; Ngai, Yim-yu. “Assessing alpha globin gene amplification and its modification of beta thalassemia phenotype.” 2015. Web. 28 Mar 2020.

Vancouver:

倪艷茹; Ngai Y. Assessing alpha globin gene amplification and its modification of beta thalassemia phenotype. [Internet] [Masters thesis]. University of Hong Kong; 2015. [cited 2020 Mar 28]. Available from: Ngai, Y. [倪艷茹]. (2015). Assessing alpha globin gene amplification and its modification of beta thalassemia phenotype. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5659400 ; http://hdl.handle.net/10722/221500.

Council of Science Editors:

倪艷茹; Ngai Y. Assessing alpha globin gene amplification and its modification of beta thalassemia phenotype. [Masters Thesis]. University of Hong Kong; 2015. Available from: Ngai, Y. [倪艷茹]. (2015). Assessing alpha globin gene amplification and its modification of beta thalassemia phenotype. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5659400 ; http://hdl.handle.net/10722/221500


University of Hong Kong

6. 馬慰平; Ma, Victor. Laboratory diagnosis of ( – SEA) alpha-thalassaemia deletion.

Degree: Master of Medical Sciences, 2001, University of Hong Kong

published_or_final_version

Medical Sciences

Master

Master of Medical Sciences

Subjects/Keywords: Thalassemia - Diagnosis.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

馬慰平; Ma, V. (2001). Laboratory diagnosis of ( – SEA) alpha-thalassaemia deletion. (Masters Thesis). University of Hong Kong. Retrieved from Ma, V. [馬慰平]. (2001). Laboratory diagnosis of ( – SEA) alpha-thalassaemia deletion. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3197006 ; http://dx.doi.org/10.5353/th_b3197006 ; http://hdl.handle.net/10722/26078

Chicago Manual of Style (16th Edition):

馬慰平; Ma, Victor. “Laboratory diagnosis of ( – SEA) alpha-thalassaemia deletion.” 2001. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. Ma, V. [馬慰平]. (2001). Laboratory diagnosis of ( – SEA) alpha-thalassaemia deletion. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3197006 ; http://dx.doi.org/10.5353/th_b3197006 ; http://hdl.handle.net/10722/26078.

MLA Handbook (7th Edition):

馬慰平; Ma, Victor. “Laboratory diagnosis of ( – SEA) alpha-thalassaemia deletion.” 2001. Web. 28 Mar 2020.

Vancouver:

馬慰平; Ma V. Laboratory diagnosis of ( – SEA) alpha-thalassaemia deletion. [Internet] [Masters thesis]. University of Hong Kong; 2001. [cited 2020 Mar 28]. Available from: Ma, V. [馬慰平]. (2001). Laboratory diagnosis of ( – SEA) alpha-thalassaemia deletion. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3197006 ; http://dx.doi.org/10.5353/th_b3197006 ; http://hdl.handle.net/10722/26078.

Council of Science Editors:

馬慰平; Ma V. Laboratory diagnosis of ( – SEA) alpha-thalassaemia deletion. [Masters Thesis]. University of Hong Kong; 2001. Available from: Ma, V. [馬慰平]. (2001). Laboratory diagnosis of ( – SEA) alpha-thalassaemia deletion. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3197006 ; http://dx.doi.org/10.5353/th_b3197006 ; http://hdl.handle.net/10722/26078


University of Hong Kong

7. Dee, Cathleen Michelle Ang. Sublethal iron overload can alter the morphology and function of dendritic cells which may predispose to gram-negative infection in beta-thalassemia.

Degree: PhD, 2014, University of Hong Kong

 Iron overload is the most common complication in transfusion-dependent thalassemias. Iron overloaded patients are frequently susceptible to gram-negative organisms such as Klebsiella pneumonaie. Literature has… (more)

Subjects/Keywords: Thalassemia; Dendritic cells; Iron - Pathophysiology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Dee, C. M. A. (2014). Sublethal iron overload can alter the morphology and function of dendritic cells which may predispose to gram-negative infection in beta-thalassemia. (Doctoral Dissertation). University of Hong Kong. Retrieved from Dee, C. M. A. [李明芳]. (2014). Sublethal iron overload can alter the morphology and function of dendritic cells which may predispose to gram-negative infection in beta-thalassemia. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5387950 ; http://dx.doi.org/10.5353/th_b5387950 ; http://hdl.handle.net/10722/221235

Chicago Manual of Style (16th Edition):

Dee, Cathleen Michelle Ang. “Sublethal iron overload can alter the morphology and function of dendritic cells which may predispose to gram-negative infection in beta-thalassemia.” 2014. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Dee, C. M. A. [李明芳]. (2014). Sublethal iron overload can alter the morphology and function of dendritic cells which may predispose to gram-negative infection in beta-thalassemia. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5387950 ; http://dx.doi.org/10.5353/th_b5387950 ; http://hdl.handle.net/10722/221235.

MLA Handbook (7th Edition):

Dee, Cathleen Michelle Ang. “Sublethal iron overload can alter the morphology and function of dendritic cells which may predispose to gram-negative infection in beta-thalassemia.” 2014. Web. 28 Mar 2020.

Vancouver:

Dee CMA. Sublethal iron overload can alter the morphology and function of dendritic cells which may predispose to gram-negative infection in beta-thalassemia. [Internet] [Doctoral dissertation]. University of Hong Kong; 2014. [cited 2020 Mar 28]. Available from: Dee, C. M. A. [李明芳]. (2014). Sublethal iron overload can alter the morphology and function of dendritic cells which may predispose to gram-negative infection in beta-thalassemia. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5387950 ; http://dx.doi.org/10.5353/th_b5387950 ; http://hdl.handle.net/10722/221235.

Council of Science Editors:

Dee CMA. Sublethal iron overload can alter the morphology and function of dendritic cells which may predispose to gram-negative infection in beta-thalassemia. [Doctoral Dissertation]. University of Hong Kong; 2014. Available from: Dee, C. M. A. [李明芳]. (2014). Sublethal iron overload can alter the morphology and function of dendritic cells which may predispose to gram-negative infection in beta-thalassemia. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5387950 ; http://dx.doi.org/10.5353/th_b5387950 ; http://hdl.handle.net/10722/221235


University of Hong Kong

8. 劉嘉媛.; Liu, Ka-wun, Ada. Detection of uncommon globin gene mutations causing unexplained microcytosis in Chinese.

Degree: Master of Medical Sciences, 2012, University of Hong Kong

The thalassaemias are the commonest monogenic disorders in the world population. They occur at a particularly high frequency in Mediterranean regions and Southeast Asia, which… (more)

Subjects/Keywords: Globin genes.; Thalassemia - Genetic aspects.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

劉嘉媛.; Liu, Ka-wun, A. (2012). Detection of uncommon globin gene mutations causing unexplained microcytosis in Chinese. (Masters Thesis). University of Hong Kong. Retrieved from Liu, K. A. [劉嘉媛]. (2012). Detection of uncommon globin gene mutations causing unexplained microcytosis in Chinese. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4842128 ; http://dx.doi.org/10.5353/th_b4842128 ; http://hdl.handle.net/10722/177293

Chicago Manual of Style (16th Edition):

劉嘉媛.; Liu, Ka-wun, Ada. “Detection of uncommon globin gene mutations causing unexplained microcytosis in Chinese.” 2012. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. Liu, K. A. [劉嘉媛]. (2012). Detection of uncommon globin gene mutations causing unexplained microcytosis in Chinese. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4842128 ; http://dx.doi.org/10.5353/th_b4842128 ; http://hdl.handle.net/10722/177293.

MLA Handbook (7th Edition):

劉嘉媛.; Liu, Ka-wun, Ada. “Detection of uncommon globin gene mutations causing unexplained microcytosis in Chinese.” 2012. Web. 28 Mar 2020.

Vancouver:

劉嘉媛.; Liu, Ka-wun A. Detection of uncommon globin gene mutations causing unexplained microcytosis in Chinese. [Internet] [Masters thesis]. University of Hong Kong; 2012. [cited 2020 Mar 28]. Available from: Liu, K. A. [劉嘉媛]. (2012). Detection of uncommon globin gene mutations causing unexplained microcytosis in Chinese. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4842128 ; http://dx.doi.org/10.5353/th_b4842128 ; http://hdl.handle.net/10722/177293.

Council of Science Editors:

劉嘉媛.; Liu, Ka-wun A. Detection of uncommon globin gene mutations causing unexplained microcytosis in Chinese. [Masters Thesis]. University of Hong Kong; 2012. Available from: Liu, K. A. [劉嘉媛]. (2012). Detection of uncommon globin gene mutations causing unexplained microcytosis in Chinese. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4842128 ; http://dx.doi.org/10.5353/th_b4842128 ; http://hdl.handle.net/10722/177293


University of Hong Kong

9. 曾皓言; Tsang, Ho-yin. Detection of clinically silent beta-globin gene mutations in Chinese using high resolution melting analysis.

Degree: Master of Medical Sciences, 2012, University of Hong Kong

Mutations in the beta-globin (β-globin) gene cause beta-thalassaemia (β-thalassaemia).The screening strategy for β-thalassaemiais based on the value of mean corpuscular volume (MCV) from the complete… (more)

Subjects/Keywords: Thalassemia - Genetic aspects.; Globin genes.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

曾皓言; Tsang, H. (2012). Detection of clinically silent beta-globin gene mutations in Chinese using high resolution melting analysis. (Masters Thesis). University of Hong Kong. Retrieved from Tsang, H. [曾皓言]. (2012). Detection of clinically silent beta-globin gene mutations in Chinese using high resolution melting analysis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4833418 ; http://dx.doi.org/10.5353/th_b4833418 ; http://hdl.handle.net/10722/173853

Chicago Manual of Style (16th Edition):

曾皓言; Tsang, Ho-yin. “Detection of clinically silent beta-globin gene mutations in Chinese using high resolution melting analysis.” 2012. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. Tsang, H. [曾皓言]. (2012). Detection of clinically silent beta-globin gene mutations in Chinese using high resolution melting analysis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4833418 ; http://dx.doi.org/10.5353/th_b4833418 ; http://hdl.handle.net/10722/173853.

MLA Handbook (7th Edition):

曾皓言; Tsang, Ho-yin. “Detection of clinically silent beta-globin gene mutations in Chinese using high resolution melting analysis.” 2012. Web. 28 Mar 2020.

Vancouver:

曾皓言; Tsang H. Detection of clinically silent beta-globin gene mutations in Chinese using high resolution melting analysis. [Internet] [Masters thesis]. University of Hong Kong; 2012. [cited 2020 Mar 28]. Available from: Tsang, H. [曾皓言]. (2012). Detection of clinically silent beta-globin gene mutations in Chinese using high resolution melting analysis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4833418 ; http://dx.doi.org/10.5353/th_b4833418 ; http://hdl.handle.net/10722/173853.

Council of Science Editors:

曾皓言; Tsang H. Detection of clinically silent beta-globin gene mutations in Chinese using high resolution melting analysis. [Masters Thesis]. University of Hong Kong; 2012. Available from: Tsang, H. [曾皓言]. (2012). Detection of clinically silent beta-globin gene mutations in Chinese using high resolution melting analysis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4833418 ; http://dx.doi.org/10.5353/th_b4833418 ; http://hdl.handle.net/10722/173853

10. Sapkal, Hemant P. Some aspects of Thalassemia: a perspective study.

Degree: Zoology, 2013, Sant Gadge Baba Amravati University

None

Bibliography p. 130-157

Advisors/Committee Members: Kulkarni, K M.

Subjects/Keywords: Zoology; Thalassemia

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Sapkal, H. P. (2013). Some aspects of Thalassemia: a perspective study. (Thesis). Sant Gadge Baba Amravati University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/10324

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Sapkal, Hemant P. “Some aspects of Thalassemia: a perspective study.” 2013. Thesis, Sant Gadge Baba Amravati University. Accessed March 28, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/10324.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Sapkal, Hemant P. “Some aspects of Thalassemia: a perspective study.” 2013. Web. 28 Mar 2020.

Vancouver:

Sapkal HP. Some aspects of Thalassemia: a perspective study. [Internet] [Thesis]. Sant Gadge Baba Amravati University; 2013. [cited 2020 Mar 28]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/10324.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Sapkal HP. Some aspects of Thalassemia: a perspective study. [Thesis]. Sant Gadge Baba Amravati University; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/10324

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

11. Nawanwat Chainuwong Pattaranggoon. Computational Study of Alpha-globin Constant Spring Structure and Binding Affinity to Alpha Haemoglobin Stabilising Protein at an Early Phase of Haemoglobin Formation .

Degree: คณะแพทยศาสตร์ ภาควิชาชีวเวชศาสตร์, 2016, Prince of Songkla University

Subjects/Keywords: Hemoglobinopathy; Thalassemia

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Pattaranggoon, N. C. (2016). Computational Study of Alpha-globin Constant Spring Structure and Binding Affinity to Alpha Haemoglobin Stabilising Protein at an Early Phase of Haemoglobin Formation . (Thesis). Prince of Songkla University. Retrieved from http://kb.psu.ac.th/psukb/handle/2016/11650

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Pattaranggoon, Nawanwat Chainuwong. “Computational Study of Alpha-globin Constant Spring Structure and Binding Affinity to Alpha Haemoglobin Stabilising Protein at an Early Phase of Haemoglobin Formation .” 2016. Thesis, Prince of Songkla University. Accessed March 28, 2020. http://kb.psu.ac.th/psukb/handle/2016/11650.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Pattaranggoon, Nawanwat Chainuwong. “Computational Study of Alpha-globin Constant Spring Structure and Binding Affinity to Alpha Haemoglobin Stabilising Protein at an Early Phase of Haemoglobin Formation .” 2016. Web. 28 Mar 2020.

Vancouver:

Pattaranggoon NC. Computational Study of Alpha-globin Constant Spring Structure and Binding Affinity to Alpha Haemoglobin Stabilising Protein at an Early Phase of Haemoglobin Formation . [Internet] [Thesis]. Prince of Songkla University; 2016. [cited 2020 Mar 28]. Available from: http://kb.psu.ac.th/psukb/handle/2016/11650.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Pattaranggoon NC. Computational Study of Alpha-globin Constant Spring Structure and Binding Affinity to Alpha Haemoglobin Stabilising Protein at an Early Phase of Haemoglobin Formation . [Thesis]. Prince of Songkla University; 2016. Available from: http://kb.psu.ac.th/psukb/handle/2016/11650

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Hong Kong

12. Lee, Ching-fung. An investigation into the effects of alpha thalassaemia on haemoglobin E level by high performance liquid chromatography in heterogeneous haemoglobin E carrier in Hong Kong.

Degree: Master of Medical Sciences, 2017, University of Hong Kong

BACKGROUND: Thalassaemia is an inherited blood disorder characterised by reduced α- and β-globin chain production and imbalance due to the defects of globin alleles. It… (more)

Subjects/Keywords: Thalassemia; Hemoglobin; High performance liquid chromatography

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Lee, C. (2017). An investigation into the effects of alpha thalassaemia on haemoglobin E level by high performance liquid chromatography in heterogeneous haemoglobin E carrier in Hong Kong. (Masters Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/251341

Chicago Manual of Style (16th Edition):

Lee, Ching-fung. “An investigation into the effects of alpha thalassaemia on haemoglobin E level by high performance liquid chromatography in heterogeneous haemoglobin E carrier in Hong Kong.” 2017. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. http://hdl.handle.net/10722/251341.

MLA Handbook (7th Edition):

Lee, Ching-fung. “An investigation into the effects of alpha thalassaemia on haemoglobin E level by high performance liquid chromatography in heterogeneous haemoglobin E carrier in Hong Kong.” 2017. Web. 28 Mar 2020.

Vancouver:

Lee C. An investigation into the effects of alpha thalassaemia on haemoglobin E level by high performance liquid chromatography in heterogeneous haemoglobin E carrier in Hong Kong. [Internet] [Masters thesis]. University of Hong Kong; 2017. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10722/251341.

Council of Science Editors:

Lee C. An investigation into the effects of alpha thalassaemia on haemoglobin E level by high performance liquid chromatography in heterogeneous haemoglobin E carrier in Hong Kong. [Masters Thesis]. University of Hong Kong; 2017. Available from: http://hdl.handle.net/10722/251341


University of Southern California

13. Brewer, Casey John. Sex differences in iron overload.

Degree: PhD, Integrative Biology of Disease, 2014, University of Southern California

 Nearly every living organism requires iron due to its roles in DNA synthesis, cellular respiration and oxygen transport. However, iron’s ability to generate free radicals… (more)

Subjects/Keywords: iron overload; thalassemia; hemochromatosis; sex steroid

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Brewer, C. J. (2014). Sex differences in iron overload. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/377382/rec/5803

Chicago Manual of Style (16th Edition):

Brewer, Casey John. “Sex differences in iron overload.” 2014. Doctoral Dissertation, University of Southern California. Accessed March 28, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/377382/rec/5803.

MLA Handbook (7th Edition):

Brewer, Casey John. “Sex differences in iron overload.” 2014. Web. 28 Mar 2020.

Vancouver:

Brewer CJ. Sex differences in iron overload. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2020 Mar 28]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/377382/rec/5803.

Council of Science Editors:

Brewer CJ. Sex differences in iron overload. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/377382/rec/5803


University of Cincinnati

14. FREEMAN, AIMEE MICHELLE. A Multicausal Approach to the Etiology of Porotic Hyperostosis at Lerna.

Degree: MA, Arts and Sciences : Anthropology, 2008, University of Cincinnati

 J. Lawrence Angel ascribed thalassemia to all instances of porotic hyperostosis at Lerna. Research has since shifted away from a single-causal etiology of porotic hyperostosis… (more)

Subjects/Keywords: Physical Anthropology; porotic hyperostosis; anemia; thalassemia; Lerna

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

FREEMAN, A. M. (2008). A Multicausal Approach to the Etiology of Porotic Hyperostosis at Lerna. (Masters Thesis). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1211564133

Chicago Manual of Style (16th Edition):

FREEMAN, AIMEE MICHELLE. “A Multicausal Approach to the Etiology of Porotic Hyperostosis at Lerna.” 2008. Masters Thesis, University of Cincinnati. Accessed March 28, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1211564133.

MLA Handbook (7th Edition):

FREEMAN, AIMEE MICHELLE. “A Multicausal Approach to the Etiology of Porotic Hyperostosis at Lerna.” 2008. Web. 28 Mar 2020.

Vancouver:

FREEMAN AM. A Multicausal Approach to the Etiology of Porotic Hyperostosis at Lerna. [Internet] [Masters thesis]. University of Cincinnati; 2008. [cited 2020 Mar 28]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1211564133.

Council of Science Editors:

FREEMAN AM. A Multicausal Approach to the Etiology of Porotic Hyperostosis at Lerna. [Masters Thesis]. University of Cincinnati; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1211564133

15. Pabbaraju, Akhila. ThalPal Android App - A medication alarm app to enhance medication adherence in adolescents with Thalassemia .

Degree: 2015, California State University – San Marcos

 Mobile health describes the use of portable electronic devices with software applications to provide health services and manage patient information. With almost 5 billion mobile… (more)

Subjects/Keywords: Thalassemia; mHealth app; Medication reminder; Medication Adherence

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Pabbaraju, A. (2015). ThalPal Android App - A medication alarm app to enhance medication adherence in adolescents with Thalassemia . (Thesis). California State University – San Marcos. Retrieved from http://hdl.handle.net/10211.3/138830

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Pabbaraju, Akhila. “ThalPal Android App - A medication alarm app to enhance medication adherence in adolescents with Thalassemia .” 2015. Thesis, California State University – San Marcos. Accessed March 28, 2020. http://hdl.handle.net/10211.3/138830.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Pabbaraju, Akhila. “ThalPal Android App - A medication alarm app to enhance medication adherence in adolescents with Thalassemia .” 2015. Web. 28 Mar 2020.

Vancouver:

Pabbaraju A. ThalPal Android App - A medication alarm app to enhance medication adherence in adolescents with Thalassemia . [Internet] [Thesis]. California State University – San Marcos; 2015. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10211.3/138830.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Pabbaraju A. ThalPal Android App - A medication alarm app to enhance medication adherence in adolescents with Thalassemia . [Thesis]. California State University – San Marcos; 2015. Available from: http://hdl.handle.net/10211.3/138830

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


McGill University

16. Popovich, Bradley W. Molecular characterization of an atypical B-thalassemia.

Degree: PhD, Department of Biology., 1986, McGill University

Subjects/Keywords: Thalassemia.; Molecular genetics.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Popovich, B. W. (1986). Molecular characterization of an atypical B-thalassemia. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile72818.pdf

Chicago Manual of Style (16th Edition):

Popovich, Bradley W. “Molecular characterization of an atypical B-thalassemia.” 1986. Doctoral Dissertation, McGill University. Accessed March 28, 2020. http://digitool.library.mcgill.ca/thesisfile72818.pdf.

MLA Handbook (7th Edition):

Popovich, Bradley W. “Molecular characterization of an atypical B-thalassemia.” 1986. Web. 28 Mar 2020.

Vancouver:

Popovich BW. Molecular characterization of an atypical B-thalassemia. [Internet] [Doctoral dissertation]. McGill University; 1986. [cited 2020 Mar 28]. Available from: http://digitool.library.mcgill.ca/thesisfile72818.pdf.

Council of Science Editors:

Popovich BW. Molecular characterization of an atypical B-thalassemia. [Doctoral Dissertation]. McGill University; 1986. Available from: http://digitool.library.mcgill.ca/thesisfile72818.pdf


McGill University

17. Heath, V. Ann. A screening program for the detection of beta thalassemia heterozygotes.

Degree: MS, Department of Biology, 1974, McGill University

Subjects/Keywords: Thalassemia.; Medical genetics.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Heath, V. A. (1974). A screening program for the detection of beta thalassemia heterozygotes. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile51896.pdf

Chicago Manual of Style (16th Edition):

Heath, V Ann. “A screening program for the detection of beta thalassemia heterozygotes.” 1974. Masters Thesis, McGill University. Accessed March 28, 2020. http://digitool.library.mcgill.ca/thesisfile51896.pdf.

MLA Handbook (7th Edition):

Heath, V Ann. “A screening program for the detection of beta thalassemia heterozygotes.” 1974. Web. 28 Mar 2020.

Vancouver:

Heath VA. A screening program for the detection of beta thalassemia heterozygotes. [Internet] [Masters thesis]. McGill University; 1974. [cited 2020 Mar 28]. Available from: http://digitool.library.mcgill.ca/thesisfile51896.pdf.

Council of Science Editors:

Heath VA. A screening program for the detection of beta thalassemia heterozygotes. [Masters Thesis]. McGill University; 1974. Available from: http://digitool.library.mcgill.ca/thesisfile51896.pdf


University of Debrecen

18. Kazemi Mohammadi, Seyedeh Maral. Pharmacotherapy of Beta Thalassemia Major .

Degree: DE – Gyógyszerésztudományi Kar, University of Debrecen

 The aim of this thesis is to discuss the incidence, aetiology, clinical manifestation, diagnosis and pharmacological management of beta thalassemia major. Beta thalassemia is caused… (more)

Subjects/Keywords: Thalassemia Major; Microcytic Anemia; Beta Thalassemia

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Kazemi Mohammadi, S. M. (n.d.). Pharmacotherapy of Beta Thalassemia Major . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/263377

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kazemi Mohammadi, Seyedeh Maral. “Pharmacotherapy of Beta Thalassemia Major .” Thesis, University of Debrecen. Accessed March 28, 2020. http://hdl.handle.net/2437/263377.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kazemi Mohammadi, Seyedeh Maral. “Pharmacotherapy of Beta Thalassemia Major .” Web. 28 Mar 2020.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Kazemi Mohammadi SM. Pharmacotherapy of Beta Thalassemia Major . [Internet] [Thesis]. University of Debrecen; [cited 2020 Mar 28]. Available from: http://hdl.handle.net/2437/263377.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Kazemi Mohammadi SM. Pharmacotherapy of Beta Thalassemia Major . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/263377

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


Universidade do Rio Grande do Norte

19. Silveira, Zama Messala Luna da. Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta .

Degree: 2010, Universidade do Rio Grande do Norte

 Beta thalassemia arises as a consequence of the reduction (β+, β++, βsilent) or absence (β0) of beta globin chain synthesis and results from a number… (more)

Subjects/Keywords: Talassemia beta; Hemoglobinopatias; Interação hemoglobina S/talassemia beta; Mutações; PCR/RFLP; β; -thalassemia; Hemoglobinopathies; S-β; thalassemia; Mutations; PCR/RFLP

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Silveira, Z. M. L. d. (2010). Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta . (Thesis). Universidade do Rio Grande do Norte. Retrieved from http://repositorio.ufrn.br/handle/123456789/13454

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Silveira, Zama Messala Luna da. “Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta .” 2010. Thesis, Universidade do Rio Grande do Norte. Accessed March 28, 2020. http://repositorio.ufrn.br/handle/123456789/13454.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Silveira, Zama Messala Luna da. “Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta .” 2010. Web. 28 Mar 2020.

Vancouver:

Silveira ZMLd. Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta . [Internet] [Thesis]. Universidade do Rio Grande do Norte; 2010. [cited 2020 Mar 28]. Available from: http://repositorio.ufrn.br/handle/123456789/13454.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Silveira ZMLd. Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta . [Thesis]. Universidade do Rio Grande do Norte; 2010. Available from: http://repositorio.ufrn.br/handle/123456789/13454

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

20. Zama Messala Luna da Silveira. Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta.

Degree: 2010, Universidade Federal do Rio Grande do Norte

Beta thalassemia arises as a consequence of the reduction (β+, β++, βsilent) or absence (β0) of beta globin chain synthesis and results from a number… (more)

Subjects/Keywords: Talassemia beta; Hemoglobinopatias; Interação hemoglobina S/talassemia beta; Mutações; PCR/RFLP; FARMACIA; β; -thalassemia; Hemoglobinopathies; S-β; thalassemia; Mutations; PCR/RFLP

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Silveira, Z. M. L. d. (2010). Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta. (Thesis). Universidade Federal do Rio Grande do Norte. Retrieved from http://bdtd.bczm.ufrn.br/tedesimplificado//tde_busca/arquivo.php?codArquivo=3759

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Silveira, Zama Messala Luna da. “Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta.” 2010. Thesis, Universidade Federal do Rio Grande do Norte. Accessed March 28, 2020. http://bdtd.bczm.ufrn.br/tedesimplificado//tde_busca/arquivo.php?codArquivo=3759.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Silveira, Zama Messala Luna da. “Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta.” 2010. Web. 28 Mar 2020.

Vancouver:

Silveira ZMLd. Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta. [Internet] [Thesis]. Universidade Federal do Rio Grande do Norte; 2010. [cited 2020 Mar 28]. Available from: http://bdtd.bczm.ufrn.br/tedesimplificado//tde_busca/arquivo.php?codArquivo=3759.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Silveira ZMLd. Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta. [Thesis]. Universidade Federal do Rio Grande do Norte; 2010. Available from: http://bdtd.bczm.ufrn.br/tedesimplificado//tde_busca/arquivo.php?codArquivo=3759

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

21. Viviani, Nilceia Maria. Avaliação dos parâmetros bioquímicos e hematológicos associados ao estudo molecular para caracterização da beta-talassemia heterozigótica.

Degree: Mestrado, Fisiopatologia Experimental, 2008, University of São Paulo

Talassemias são as mais comuns desordens monogenéticas em humanos; são caracterizadas pela presença de anemia microcíticas e hipocrômicas que resultam da redução ou ausência na… (more)

Subjects/Keywords: Beta-thalassemia; Brasil; Brazil; Mutação; Mutation; Talassemia; Talassemia-beta; Techniques and procedures; Técnicas e procedimentos de laboratório; Thalassemia

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Viviani, N. M. (2008). Avaliação dos parâmetros bioquímicos e hematológicos associados ao estudo molecular para caracterização da beta-talassemia heterozigótica. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5160/tde-30012009-165046/ ;

Chicago Manual of Style (16th Edition):

Viviani, Nilceia Maria. “Avaliação dos parâmetros bioquímicos e hematológicos associados ao estudo molecular para caracterização da beta-talassemia heterozigótica.” 2008. Masters Thesis, University of São Paulo. Accessed March 28, 2020. http://www.teses.usp.br/teses/disponiveis/5/5160/tde-30012009-165046/ ;.

MLA Handbook (7th Edition):

Viviani, Nilceia Maria. “Avaliação dos parâmetros bioquímicos e hematológicos associados ao estudo molecular para caracterização da beta-talassemia heterozigótica.” 2008. Web. 28 Mar 2020.

Vancouver:

Viviani NM. Avaliação dos parâmetros bioquímicos e hematológicos associados ao estudo molecular para caracterização da beta-talassemia heterozigótica. [Internet] [Masters thesis]. University of São Paulo; 2008. [cited 2020 Mar 28]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-30012009-165046/ ;.

Council of Science Editors:

Viviani NM. Avaliação dos parâmetros bioquímicos e hematológicos associados ao estudo molecular para caracterização da beta-talassemia heterozigótica. [Masters Thesis]. University of São Paulo; 2008. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-30012009-165046/ ;


University of Hong Kong

22. Li, Ming-cheng, Anita. {221} thalassaemia in Hong Kong children.

Degree: Doctor of Medicine, 1998, University of Hong Kong

published_or_final_version

Medicine

Master

Doctor of Medicine

Subjects/Keywords: Thalassemia in children - China - Hong Kong.; Thalassemia in children.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Li, Ming-cheng, A. (1998). {221} thalassaemia in Hong Kong children. (Doctoral Dissertation). University of Hong Kong. Retrieved from Li, M. A. [李明眞]. (1998). β thalassaemia in Hong Kong children. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4389387 ; http://dx.doi.org/10.5353/th_b4389387 ; http://hdl.handle.net/10722/65095

Chicago Manual of Style (16th Edition):

Li, Ming-cheng, Anita. “{221} thalassaemia in Hong Kong children.” 1998. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Li, M. A. [李明眞]. (1998). β thalassaemia in Hong Kong children. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4389387 ; http://dx.doi.org/10.5353/th_b4389387 ; http://hdl.handle.net/10722/65095.

MLA Handbook (7th Edition):

Li, Ming-cheng, Anita. “{221} thalassaemia in Hong Kong children.” 1998. Web. 28 Mar 2020.

Vancouver:

Li, Ming-cheng A. {221} thalassaemia in Hong Kong children. [Internet] [Doctoral dissertation]. University of Hong Kong; 1998. [cited 2020 Mar 28]. Available from: Li, M. A. [李明眞]. (1998). β thalassaemia in Hong Kong children. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4389387 ; http://dx.doi.org/10.5353/th_b4389387 ; http://hdl.handle.net/10722/65095.

Council of Science Editors:

Li, Ming-cheng A. {221} thalassaemia in Hong Kong children. [Doctoral Dissertation]. University of Hong Kong; 1998. Available from: Li, M. A. [李明眞]. (1998). β thalassaemia in Hong Kong children. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4389387 ; http://dx.doi.org/10.5353/th_b4389387 ; http://hdl.handle.net/10722/65095

23. Trompoukis, Christos. Καρδιολογική μελέτη μικροδρεπανοκυτταρικής αναιμίας.

Degree: 2014, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

Purpose: Cardiovascular involvement is a leading cause of mortality and morbidity inpatients with inherited hemoglobinopathies and attracts increasing interest in theliterature, in the light of… (more)

Subjects/Keywords: Δρεπανοκυτταρική νόσος; Θαλασσαιμία; Μικροδρεπανοκυτταρική αναιμία; Πνευμονική υπέρταση; Καρδιακή ανεπάρκεια; Sickle cell disease; Thalassemia; Sickle b - thalassemia; Pulmonary hypertension; Heart failure

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Trompoukis, C. (2014). Καρδιολογική μελέτη μικροδρεπανοκυτταρικής αναιμίας. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/42068

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Trompoukis, Christos. “Καρδιολογική μελέτη μικροδρεπανοκυτταρικής αναιμίας.” 2014. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed March 28, 2020. http://hdl.handle.net/10442/hedi/42068.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Trompoukis, Christos. “Καρδιολογική μελέτη μικροδρεπανοκυτταρικής αναιμίας.” 2014. Web. 28 Mar 2020.

Vancouver:

Trompoukis C. Καρδιολογική μελέτη μικροδρεπανοκυτταρικής αναιμίας. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10442/hedi/42068.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Trompoukis C. Καρδιολογική μελέτη μικροδρεπανοκυτταρικής αναιμίας. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. Available from: http://hdl.handle.net/10442/hedi/42068

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universidade do Rio Grande do Norte

24. Silveira, Zama Messala Luna da. Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta .

Degree: 2010, Universidade do Rio Grande do Norte

 Beta thalassemia arises as a consequence of the reduction (β+, β++, βsilent) or absence (β0) of beta globin chain synthesis and results from a number… (more)

Subjects/Keywords: Talassemia beta; Hemoglobinopatias; Interação hemoglobina S/talassemia beta; Mutações; PCR/RFLP; β; -thalassemia; Hemoglobinopathies; S-β; thalassemia; Mutations; PCR/RFLP

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Silveira, Z. M. L. d. (2010). Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta . (Masters Thesis). Universidade do Rio Grande do Norte. Retrieved from http://repositorio.ufrn.br/handle/123456789/13454

Chicago Manual of Style (16th Edition):

Silveira, Zama Messala Luna da. “Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta .” 2010. Masters Thesis, Universidade do Rio Grande do Norte. Accessed March 28, 2020. http://repositorio.ufrn.br/handle/123456789/13454.

MLA Handbook (7th Edition):

Silveira, Zama Messala Luna da. “Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta .” 2010. Web. 28 Mar 2020.

Vancouver:

Silveira ZMLd. Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta . [Internet] [Masters thesis]. Universidade do Rio Grande do Norte; 2010. [cited 2020 Mar 28]. Available from: http://repositorio.ufrn.br/handle/123456789/13454.

Council of Science Editors:

Silveira ZMLd. Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta . [Masters Thesis]. Universidade do Rio Grande do Norte; 2010. Available from: http://repositorio.ufrn.br/handle/123456789/13454


Universidade do Rio Grande do Norte

25. Silveira, Zama Messala Luna da. Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta .

Degree: 2010, Universidade do Rio Grande do Norte

 Beta thalassemia arises as a consequence of the reduction (β+, β++, βsilent) or absence (β0) of beta globin chain synthesis and results from a number… (more)

Subjects/Keywords: Talassemia beta; Hemoglobinopatias; Interação hemoglobina S/talassemia beta; Mutações; PCR/RFLP; β; -thalassemia; Hemoglobinopathies; S-β; thalassemia; Mutations; PCR/RFLP

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Silveira, Z. M. L. d. (2010). Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta . (Masters Thesis). Universidade do Rio Grande do Norte. Retrieved from http://repositorio.ufrn.br/handle/123456789/13454

Chicago Manual of Style (16th Edition):

Silveira, Zama Messala Luna da. “Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta .” 2010. Masters Thesis, Universidade do Rio Grande do Norte. Accessed March 28, 2020. http://repositorio.ufrn.br/handle/123456789/13454.

MLA Handbook (7th Edition):

Silveira, Zama Messala Luna da. “Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta .” 2010. Web. 28 Mar 2020.

Vancouver:

Silveira ZMLd. Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta . [Internet] [Masters thesis]. Universidade do Rio Grande do Norte; 2010. [cited 2020 Mar 28]. Available from: http://repositorio.ufrn.br/handle/123456789/13454.

Council of Science Editors:

Silveira ZMLd. Caracterização molecular e laboratorial da talassemia beta e da interação hemoglobina s/talassemia beta . [Masters Thesis]. Universidade do Rio Grande do Norte; 2010. Available from: http://repositorio.ufrn.br/handle/123456789/13454

26. Παΐζη, Αρσινόη. Φαρμακογονιδιωματική και λειτουργική μελέτη συσχέτισης μικροδορυφορικών αλληλουχιών στον υποκινητή του γονιδίου MAP3K5 με τα επίπεδα μεταγραφής του γονιδίου.

Degree: 2013, University of Patras

Γενετικές παραλλαγές σε γονιδιακούς τόπους που βρίσκονται εντός (cis) αλλά και εκτός (trans) του συμπλέγματος των ανθρώπινων β-σφαιρινικών γονιδίων έχει δειχθεί πως συσχετίζονται σημαντικά με… (more)

Subjects/Keywords: Αιμοσφαιρίνες; β-Μεσογειακή αναιμία; 612.111 1; Hemoglobins; β-Thalassemia

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Παΐζη, . (2013). Φαρμακογονιδιωματική και λειτουργική μελέτη συσχέτισης μικροδορυφορικών αλληλουχιών στον υποκινητή του γονιδίου MAP3K5 με τα επίπεδα μεταγραφής του γονιδίου. (Masters Thesis). University of Patras. Retrieved from http://hdl.handle.net/10889/6973

Chicago Manual of Style (16th Edition):

Παΐζη, Αρσινόη. “Φαρμακογονιδιωματική και λειτουργική μελέτη συσχέτισης μικροδορυφορικών αλληλουχιών στον υποκινητή του γονιδίου MAP3K5 με τα επίπεδα μεταγραφής του γονιδίου.” 2013. Masters Thesis, University of Patras. Accessed March 28, 2020. http://hdl.handle.net/10889/6973.

MLA Handbook (7th Edition):

Παΐζη, Αρσινόη. “Φαρμακογονιδιωματική και λειτουργική μελέτη συσχέτισης μικροδορυφορικών αλληλουχιών στον υποκινητή του γονιδίου MAP3K5 με τα επίπεδα μεταγραφής του γονιδίου.” 2013. Web. 28 Mar 2020.

Vancouver:

Παΐζη . Φαρμακογονιδιωματική και λειτουργική μελέτη συσχέτισης μικροδορυφορικών αλληλουχιών στον υποκινητή του γονιδίου MAP3K5 με τα επίπεδα μεταγραφής του γονιδίου. [Internet] [Masters thesis]. University of Patras; 2013. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10889/6973.

Council of Science Editors:

Παΐζη . Φαρμακογονιδιωματική και λειτουργική μελέτη συσχέτισης μικροδορυφορικών αλληλουχιών στον υποκινητή του γονιδίου MAP3K5 με τα επίπεδα μεταγραφής του γονιδίου. [Masters Thesis]. University of Patras; 2013. Available from: http://hdl.handle.net/10889/6973

27. Μπαρτσακούλια, Μαρίνα. Μελέτη του ρόλου του γονιδίου KLF10 στην αύξηση των επιπέδων της εμβρυικής αιμοσφαιρίνης ασθενών με β-μεσογειακή αναιμία και την ανταπόκρισή τους σε υδροξυουρία.

Degree: 2013, University of Patras

Οι αιμοσφαιρινοπάθειες συγκαταλέγονται ανάμεσα στις πιο κοινές μονογονιδιακές διαταραχές παγκοσμίως, συμπεριλαμβανομένης της β-θαλασσαιμίας και της δρεπανοκυτταρικής αναιμίας. Η επανενεργοποίηση των γονιδίων της γ-σφαιρίνης φαίνεται να… (more)

Subjects/Keywords: β-μεσογειακή αναιμία; Υδροξυουρία; 616.152 042 695; β-thalassemia; Hydroxyurea (HU)

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Μπαρτσακούλια, . (2013). Μελέτη του ρόλου του γονιδίου KLF10 στην αύξηση των επιπέδων της εμβρυικής αιμοσφαιρίνης ασθενών με β-μεσογειακή αναιμία και την ανταπόκρισή τους σε υδροξυουρία. (Masters Thesis). University of Patras. Retrieved from http://hdl.handle.net/10889/6322

Chicago Manual of Style (16th Edition):

Μπαρτσακούλια, Μαρίνα. “Μελέτη του ρόλου του γονιδίου KLF10 στην αύξηση των επιπέδων της εμβρυικής αιμοσφαιρίνης ασθενών με β-μεσογειακή αναιμία και την ανταπόκρισή τους σε υδροξυουρία.” 2013. Masters Thesis, University of Patras. Accessed March 28, 2020. http://hdl.handle.net/10889/6322.

MLA Handbook (7th Edition):

Μπαρτσακούλια, Μαρίνα. “Μελέτη του ρόλου του γονιδίου KLF10 στην αύξηση των επιπέδων της εμβρυικής αιμοσφαιρίνης ασθενών με β-μεσογειακή αναιμία και την ανταπόκρισή τους σε υδροξυουρία.” 2013. Web. 28 Mar 2020.

Vancouver:

Μπαρτσακούλια . Μελέτη του ρόλου του γονιδίου KLF10 στην αύξηση των επιπέδων της εμβρυικής αιμοσφαιρίνης ασθενών με β-μεσογειακή αναιμία και την ανταπόκρισή τους σε υδροξυουρία. [Internet] [Masters thesis]. University of Patras; 2013. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10889/6322.

Council of Science Editors:

Μπαρτσακούλια . Μελέτη του ρόλου του γονιδίου KLF10 στην αύξηση των επιπέδων της εμβρυικής αιμοσφαιρίνης ασθενών με β-μεσογειακή αναιμία και την ανταπόκρισή τους σε υδροξυουρία. [Masters Thesis]. University of Patras; 2013. Available from: http://hdl.handle.net/10889/6322


University of Hong Kong

28. 陳玉燕.; Chan, Yuk-yin. Haematological and molecular studies of Thalassaemias in Hong Kong Chinese.

Degree: M. Phil., 1998, University of Hong Kong

published_or_final_version

Pathology

Master

Master of Philosophy

Subjects/Keywords: Thalassemia - China - Hong Kong.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

陳玉燕.; Chan, Y. (1998). Haematological and molecular studies of Thalassaemias in Hong Kong Chinese. (Masters Thesis). University of Hong Kong. Retrieved from Chan, Y. [陳玉燕]. (1998). Haematological and molecular studies of Thalassaemias in Hong Kong Chinese. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3121501 ; http://dx.doi.org/10.5353/th_b3121501 ; http://hdl.handle.net/10722/33247

Chicago Manual of Style (16th Edition):

陳玉燕.; Chan, Yuk-yin. “Haematological and molecular studies of Thalassaemias in Hong Kong Chinese.” 1998. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. Chan, Y. [陳玉燕]. (1998). Haematological and molecular studies of Thalassaemias in Hong Kong Chinese. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3121501 ; http://dx.doi.org/10.5353/th_b3121501 ; http://hdl.handle.net/10722/33247.

MLA Handbook (7th Edition):

陳玉燕.; Chan, Yuk-yin. “Haematological and molecular studies of Thalassaemias in Hong Kong Chinese.” 1998. Web. 28 Mar 2020.

Vancouver:

陳玉燕.; Chan Y. Haematological and molecular studies of Thalassaemias in Hong Kong Chinese. [Internet] [Masters thesis]. University of Hong Kong; 1998. [cited 2020 Mar 28]. Available from: Chan, Y. [陳玉燕]. (1998). Haematological and molecular studies of Thalassaemias in Hong Kong Chinese. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3121501 ; http://dx.doi.org/10.5353/th_b3121501 ; http://hdl.handle.net/10722/33247.

Council of Science Editors:

陳玉燕.; Chan Y. Haematological and molecular studies of Thalassaemias in Hong Kong Chinese. [Masters Thesis]. University of Hong Kong; 1998. Available from: Chan, Y. [陳玉燕]. (1998). Haematological and molecular studies of Thalassaemias in Hong Kong Chinese. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3121501 ; http://dx.doi.org/10.5353/th_b3121501 ; http://hdl.handle.net/10722/33247


University of Hong Kong

29. Leung, Kwok-yin. Prenatal ultrasound prediction of homozygous α⁰-thalassemia.

Degree: Doctor of Medicine, 2012, University of Hong Kong

 Homozygous α0-thalassemia is a serious autosomal recessive disorder with poor fetal outcome and severe maternal complications. Conventionally, prenatal diagnosis is performed by an invasive test.… (more)

Subjects/Keywords: Fetus - Ultrasonic imaging.; Thalassemia - Diagnosis.; Diagnostic ultrasonic imaging.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Leung, K. (2012). Prenatal ultrasound prediction of homozygous α⁰-thalassemia. (Doctoral Dissertation). University of Hong Kong. Retrieved from Leung, K. [梁國賢]. (2012). Prenatal ultrasound prediction of homozygous α⁰-thalassemia. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4745403 ; http://dx.doi.org/10.5353/th_b4745403 ; http://hdl.handle.net/10722/174391

Chicago Manual of Style (16th Edition):

Leung, Kwok-yin. “Prenatal ultrasound prediction of homozygous α⁰-thalassemia.” 2012. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Leung, K. [梁國賢]. (2012). Prenatal ultrasound prediction of homozygous α⁰-thalassemia. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4745403 ; http://dx.doi.org/10.5353/th_b4745403 ; http://hdl.handle.net/10722/174391.

MLA Handbook (7th Edition):

Leung, Kwok-yin. “Prenatal ultrasound prediction of homozygous α⁰-thalassemia.” 2012. Web. 28 Mar 2020.

Vancouver:

Leung K. Prenatal ultrasound prediction of homozygous α⁰-thalassemia. [Internet] [Doctoral dissertation]. University of Hong Kong; 2012. [cited 2020 Mar 28]. Available from: Leung, K. [梁國賢]. (2012). Prenatal ultrasound prediction of homozygous α⁰-thalassemia. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4745403 ; http://dx.doi.org/10.5353/th_b4745403 ; http://hdl.handle.net/10722/174391.

Council of Science Editors:

Leung K. Prenatal ultrasound prediction of homozygous α⁰-thalassemia. [Doctoral Dissertation]. University of Hong Kong; 2012. Available from: Leung, K. [梁國賢]. (2012). Prenatal ultrasound prediction of homozygous α⁰-thalassemia. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4745403 ; http://dx.doi.org/10.5353/th_b4745403 ; http://hdl.handle.net/10722/174391


University of Hong Kong

30. Tan-Un, Kian-cheng. Chinese B thalassaemia: DNA polymorphisms andspecific mutations.

Degree: PhD, 1986, University of Hong Kong

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Subjects/Keywords: Hemoglobin polymorphisms.; Thalassemia.; Animal mutation.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Tan-Un, K. (1986). Chinese B thalassaemia: DNA polymorphisms andspecific mutations. (Doctoral Dissertation). University of Hong Kong. Retrieved from Tan-Un, K. [阮陳健貞]. (1986). Chinese B thalassaemia : DNA polymorphisms and specific mutations. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3123097 ; http://dx.doi.org/10.5353/th_b3123097 ; http://hdl.handle.net/10722/34825

Chicago Manual of Style (16th Edition):

Tan-Un, Kian-cheng. “Chinese B thalassaemia: DNA polymorphisms andspecific mutations.” 1986. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Tan-Un, K. [阮陳健貞]. (1986). Chinese B thalassaemia : DNA polymorphisms and specific mutations. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3123097 ; http://dx.doi.org/10.5353/th_b3123097 ; http://hdl.handle.net/10722/34825.

MLA Handbook (7th Edition):

Tan-Un, Kian-cheng. “Chinese B thalassaemia: DNA polymorphisms andspecific mutations.” 1986. Web. 28 Mar 2020.

Vancouver:

Tan-Un K. Chinese B thalassaemia: DNA polymorphisms andspecific mutations. [Internet] [Doctoral dissertation]. University of Hong Kong; 1986. [cited 2020 Mar 28]. Available from: Tan-Un, K. [阮陳健貞]. (1986). Chinese B thalassaemia : DNA polymorphisms and specific mutations. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3123097 ; http://dx.doi.org/10.5353/th_b3123097 ; http://hdl.handle.net/10722/34825.

Council of Science Editors:

Tan-Un K. Chinese B thalassaemia: DNA polymorphisms andspecific mutations. [Doctoral Dissertation]. University of Hong Kong; 1986. Available from: Tan-Un, K. [阮陳健貞]. (1986). Chinese B thalassaemia : DNA polymorphisms and specific mutations. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3123097 ; http://dx.doi.org/10.5353/th_b3123097 ; http://hdl.handle.net/10722/34825

[1] [2] [3] [4] [5] [6]

.