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You searched for subject:(Polymorphisms). Showing records 1 – 30 of 791 total matches.

[1] [2] [3] [4] [5] … [27]

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Rutgers University

1. Misra, Ashish, 1981. Analysis of single nucleotide polymorphisms using molecular affinity separation and mass spectrometry.

Degree: PhD, Chemical and Biochemical Engineering, 2009, Rutgers University

Single nucleotide polymorphisms (SNP) constitute the most abundant human genetic variations and are important markers for studying interindividual variability with many different techniques having being… (more)

Subjects/Keywords: Genetic polymorphisms

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APA (6th Edition):

Misra, Ashish, 1. (2009). Analysis of single nucleotide polymorphisms using molecular affinity separation and mass spectrometry. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051381

Chicago Manual of Style (16th Edition):

Misra, Ashish, 1981. “Analysis of single nucleotide polymorphisms using molecular affinity separation and mass spectrometry.” 2009. Doctoral Dissertation, Rutgers University. Accessed May 26, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051381.

MLA Handbook (7th Edition):

Misra, Ashish, 1981. “Analysis of single nucleotide polymorphisms using molecular affinity separation and mass spectrometry.” 2009. Web. 26 May 2019.

Vancouver:

Misra, Ashish 1. Analysis of single nucleotide polymorphisms using molecular affinity separation and mass spectrometry. [Internet] [Doctoral dissertation]. Rutgers University; 2009. [cited 2019 May 26]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051381.

Council of Science Editors:

Misra, Ashish 1. Analysis of single nucleotide polymorphisms using molecular affinity separation and mass spectrometry. [Doctoral Dissertation]. Rutgers University; 2009. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051381


Brunel University

2. Liozidou, Maria. Genetic epidemiology of breast cancer in Cyprus : a case-control study of DNA repair genes.

Degree: 2009, Brunel University

 The occurrence of early-onset breast cancer (EOBC) has been associated with germline mutations in the BRCA1 and BRCA2 genes. The first aim of this thesis… (more)

Subjects/Keywords: 610.7343; Polymorphisms; Risk

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APA (6th Edition):

Liozidou, M. (2009). Genetic epidemiology of breast cancer in Cyprus : a case-control study of DNA repair genes. (Doctoral Dissertation). Brunel University. Retrieved from http://bura.brunel.ac.uk/handle/2438/4111 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.508838

Chicago Manual of Style (16th Edition):

Liozidou, Maria. “Genetic epidemiology of breast cancer in Cyprus : a case-control study of DNA repair genes.” 2009. Doctoral Dissertation, Brunel University. Accessed May 26, 2019. http://bura.brunel.ac.uk/handle/2438/4111 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.508838.

MLA Handbook (7th Edition):

Liozidou, Maria. “Genetic epidemiology of breast cancer in Cyprus : a case-control study of DNA repair genes.” 2009. Web. 26 May 2019.

Vancouver:

Liozidou M. Genetic epidemiology of breast cancer in Cyprus : a case-control study of DNA repair genes. [Internet] [Doctoral dissertation]. Brunel University; 2009. [cited 2019 May 26]. Available from: http://bura.brunel.ac.uk/handle/2438/4111 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.508838.

Council of Science Editors:

Liozidou M. Genetic epidemiology of breast cancer in Cyprus : a case-control study of DNA repair genes. [Doctoral Dissertation]. Brunel University; 2009. Available from: http://bura.brunel.ac.uk/handle/2438/4111 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.508838

3. Sapkota, Shraddha. Synergistic Associations of Genetic, Demographic, Health, and Lifestyle Risk Factors on Neurocognitive Performance and Change in Aging.

Degree: PhD, Centre for Neuroscience, 2016, University of Alberta

 Objective: Neurocognitive phenotypes observed in aging have been linked to select combinations of candidate genetic polymorphisms and modifiable risk factors. In this dissertation, I test… (more)

Subjects/Keywords: Aging; Neurocognitive Performance; Genetic Polymorphisms

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APA (6th Edition):

Sapkota, S. (2016). Synergistic Associations of Genetic, Demographic, Health, and Lifestyle Risk Factors on Neurocognitive Performance and Change in Aging. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/csn009x77d

Chicago Manual of Style (16th Edition):

Sapkota, Shraddha. “Synergistic Associations of Genetic, Demographic, Health, and Lifestyle Risk Factors on Neurocognitive Performance and Change in Aging.” 2016. Doctoral Dissertation, University of Alberta. Accessed May 26, 2019. https://era.library.ualberta.ca/files/csn009x77d.

MLA Handbook (7th Edition):

Sapkota, Shraddha. “Synergistic Associations of Genetic, Demographic, Health, and Lifestyle Risk Factors on Neurocognitive Performance and Change in Aging.” 2016. Web. 26 May 2019.

Vancouver:

Sapkota S. Synergistic Associations of Genetic, Demographic, Health, and Lifestyle Risk Factors on Neurocognitive Performance and Change in Aging. [Internet] [Doctoral dissertation]. University of Alberta; 2016. [cited 2019 May 26]. Available from: https://era.library.ualberta.ca/files/csn009x77d.

Council of Science Editors:

Sapkota S. Synergistic Associations of Genetic, Demographic, Health, and Lifestyle Risk Factors on Neurocognitive Performance and Change in Aging. [Doctoral Dissertation]. University of Alberta; 2016. Available from: https://era.library.ualberta.ca/files/csn009x77d


University of Pretoria

4. Ganesan, Hamilton. New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms.

Degree: Biochemistry, 2010, University of Pretoria

 Tuberculosis is one of the leading causes of mortality globally. Although this disease has been around for many generations, treatment and management of the disease… (more)

Subjects/Keywords: Nucleotide polymorphisms; Comparative genomics; UCTD

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APA (6th Edition):

Ganesan, H. (2010). New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/25245

Chicago Manual of Style (16th Edition):

Ganesan, Hamilton. “New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms.” 2010. Doctoral Dissertation, University of Pretoria. Accessed May 26, 2019. http://hdl.handle.net/2263/25245.

MLA Handbook (7th Edition):

Ganesan, Hamilton. “New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms.” 2010. Web. 26 May 2019.

Vancouver:

Ganesan H. New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms. [Internet] [Doctoral dissertation]. University of Pretoria; 2010. [cited 2019 May 26]. Available from: http://hdl.handle.net/2263/25245.

Council of Science Editors:

Ganesan H. New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms. [Doctoral Dissertation]. University of Pretoria; 2010. Available from: http://hdl.handle.net/2263/25245

5. Bhasin, Yasha. Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis.

Degree: 2009, University of Pune

Common complex disorders, also known as multifactorial disorders, are characterized by the interactions of multiple genetic and/or environmental factors that influence the expression of a… (more)

Subjects/Keywords: Biotechnology; Single Nucleotide Polymorphisms

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APA (6th Edition):

Bhasin, Y. (2009). Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis. (Thesis). University of Pune. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/3417

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):

Bhasin, Yasha. “Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis.” 2009. Thesis, University of Pune. Accessed May 26, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/3417.

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

MLA Handbook (7th Edition):

Bhasin, Yasha. “Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis.” 2009. Web. 26 May 2019.

Vancouver:

Bhasin Y. Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis. [Internet] [Thesis]. University of Pune; 2009. [cited 2019 May 26]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/3417.

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

Council of Science Editors:

Bhasin Y. Single nucleotide polymorphisms (SNPs) in complex disorders: a genome-widw computational analysis. [Thesis]. University of Pune; 2009. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/3417

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

6. Bali, Prerna. Toll like receptor polymorphisms in relation to malaria in the Indian population; -.

Degree: Zoology, 2013, University of Delhi

Available

Bibliography p.98-115, Appendix p.122-128

Advisors/Committee Members: Singh, A K and Adak, T.

Subjects/Keywords: Polymorphisms; Malaria

Page 1

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APA (6th Edition):

Bali, P. (2013). Toll like receptor polymorphisms in relation to malaria in the Indian population; -. (Thesis). University of Delhi. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/26844

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):

Bali, Prerna. “Toll like receptor polymorphisms in relation to malaria in the Indian population; -.” 2013. Thesis, University of Delhi. Accessed May 26, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/26844.

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

MLA Handbook (7th Edition):

Bali, Prerna. “Toll like receptor polymorphisms in relation to malaria in the Indian population; -.” 2013. Web. 26 May 2019.

Vancouver:

Bali P. Toll like receptor polymorphisms in relation to malaria in the Indian population; -. [Internet] [Thesis]. University of Delhi; 2013. [cited 2019 May 26]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/26844.

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

Council of Science Editors:

Bali P. Toll like receptor polymorphisms in relation to malaria in the Indian population; -. [Thesis]. University of Delhi; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/26844

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


University of Pretoria

7. [No author]. New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms .

Degree: 2010, University of Pretoria

 Tuberculosis is one of the leading causes of mortality globally. Although this disease has been around for many generations, treatment and management of the disease… (more)

Subjects/Keywords: Nucleotide polymorphisms; Comparative genomics; UCTD

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APA (6th Edition):

author], [. (2010). New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms . (Doctoral Dissertation). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-06042010-004142/

Chicago Manual of Style (16th Edition):

author], [No. “New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms .” 2010. Doctoral Dissertation, University of Pretoria. Accessed May 26, 2019. http://upetd.up.ac.za/thesis/available/etd-06042010-004142/.

MLA Handbook (7th Edition):

author], [No. “New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms .” 2010. Web. 26 May 2019.

Vancouver:

author] [. New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms . [Internet] [Doctoral dissertation]. University of Pretoria; 2010. [cited 2019 May 26]. Available from: http://upetd.up.ac.za/thesis/available/etd-06042010-004142/.

Council of Science Editors:

author] [. New tools for comparative genomics based on oligonucleotide compositional constraints and single nucleotide polymorphisms . [Doctoral Dissertation]. University of Pretoria; 2010. Available from: http://upetd.up.ac.za/thesis/available/etd-06042010-004142/


Oregon State University

8. McDonald, John H. Ecological genetics of two polymorphic enzymes in three species of Megalorchestia (Amphipoda:Talitridae).

Degree: MS, Oceanography, 1983, Oregon State University

Subjects/Keywords: Genetic polymorphisms

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APA (6th Edition):

McDonald, J. H. (1983). Ecological genetics of two polymorphic enzymes in three species of Megalorchestia (Amphipoda:Talitridae). (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/28199

Chicago Manual of Style (16th Edition):

McDonald, John H. “Ecological genetics of two polymorphic enzymes in three species of Megalorchestia (Amphipoda:Talitridae).” 1983. Masters Thesis, Oregon State University. Accessed May 26, 2019. http://hdl.handle.net/1957/28199.

MLA Handbook (7th Edition):

McDonald, John H. “Ecological genetics of two polymorphic enzymes in three species of Megalorchestia (Amphipoda:Talitridae).” 1983. Web. 26 May 2019.

Vancouver:

McDonald JH. Ecological genetics of two polymorphic enzymes in three species of Megalorchestia (Amphipoda:Talitridae). [Internet] [Masters thesis]. Oregon State University; 1983. [cited 2019 May 26]. Available from: http://hdl.handle.net/1957/28199.

Council of Science Editors:

McDonald JH. Ecological genetics of two polymorphic enzymes in three species of Megalorchestia (Amphipoda:Talitridae). [Masters Thesis]. Oregon State University; 1983. Available from: http://hdl.handle.net/1957/28199


University of Hawaii – Manoa

9. 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

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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 May 26, 2019. 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. 26 May 2019.

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 2019 May 26]. 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 Louisville

10. Connor, Avonne Elish. The beta-2 adrenergic receptor polymorphisms and risk of breast cancer among hispanic and non-hispanic white women from the 4-corners breast cancer study : a population-based case-control examination.

Degree: PhD, 2011, University of Louisville

Polymorphisms in the adrenergic receptor beta-2 (ADRB2) gene have been studied in relation to risk of Type 2 diabetes and obesity, but few studies have… (more)

Subjects/Keywords: Breast cancer; Ethnicity; Epidemiology; Polymorphisms

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APA (6th Edition):

Connor, A. E. (2011). The beta-2 adrenergic receptor polymorphisms and risk of breast cancer among hispanic and non-hispanic white women from the 4-corners breast cancer study : a population-based case-control examination. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/271 ; https://ir.library.louisville.edu/etd/271

Chicago Manual of Style (16th Edition):

Connor, Avonne Elish. “The beta-2 adrenergic receptor polymorphisms and risk of breast cancer among hispanic and non-hispanic white women from the 4-corners breast cancer study : a population-based case-control examination.” 2011. Doctoral Dissertation, University of Louisville. Accessed May 26, 2019. 10.18297/etd/271 ; https://ir.library.louisville.edu/etd/271.

MLA Handbook (7th Edition):

Connor, Avonne Elish. “The beta-2 adrenergic receptor polymorphisms and risk of breast cancer among hispanic and non-hispanic white women from the 4-corners breast cancer study : a population-based case-control examination.” 2011. Web. 26 May 2019.

Vancouver:

Connor AE. The beta-2 adrenergic receptor polymorphisms and risk of breast cancer among hispanic and non-hispanic white women from the 4-corners breast cancer study : a population-based case-control examination. [Internet] [Doctoral dissertation]. University of Louisville; 2011. [cited 2019 May 26]. Available from: 10.18297/etd/271 ; https://ir.library.louisville.edu/etd/271.

Council of Science Editors:

Connor AE. The beta-2 adrenergic receptor polymorphisms and risk of breast cancer among hispanic and non-hispanic white women from the 4-corners breast cancer study : a population-based case-control examination. [Doctoral Dissertation]. University of Louisville; 2011. Available from: 10.18297/etd/271 ; https://ir.library.louisville.edu/etd/271


Oregon State University

11. Templeton, Joe Wayne, 1941-. Genetic polymorphism of sheep hemoglobin.

Degree: PhD, Genetics, 1968, Oregon State University

 Five breeds of sheep (Columbia, Targhee, Rambouillet, Lincoln, and Suffolk) were found to possess two hemoglobin types (Hb. A and Hb. B) when their hemoglobins… (more)

Subjects/Keywords: Genetic polymorphisms

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APA (6th Edition):

Templeton, Joe Wayne, 1. (1968). Genetic polymorphism of sheep hemoglobin. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/46356

Chicago Manual of Style (16th Edition):

Templeton, Joe Wayne, 1941-. “Genetic polymorphism of sheep hemoglobin.” 1968. Doctoral Dissertation, Oregon State University. Accessed May 26, 2019. http://hdl.handle.net/1957/46356.

MLA Handbook (7th Edition):

Templeton, Joe Wayne, 1941-. “Genetic polymorphism of sheep hemoglobin.” 1968. Web. 26 May 2019.

Vancouver:

Templeton, Joe Wayne 1. Genetic polymorphism of sheep hemoglobin. [Internet] [Doctoral dissertation]. Oregon State University; 1968. [cited 2019 May 26]. Available from: http://hdl.handle.net/1957/46356.

Council of Science Editors:

Templeton, Joe Wayne 1. Genetic polymorphism of sheep hemoglobin. [Doctoral Dissertation]. Oregon State University; 1968. Available from: http://hdl.handle.net/1957/46356


University of New South Wales

12. Tang, Joyce Chi Man. Studies on the Vitamin C transporter gene SLC23A2 and cardiac conduction.

Degree: Rural Clinical School, 2017, University of New South Wales

 This thesis considers the role of Vitamin C genes on cardiac conduction. Firstly we performed a systematic literature review to ascertain the protective effects of… (more)

Subjects/Keywords: Polymorphisms; Vitamin C; Cardiac Conduction

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APA (6th Edition):

Tang, J. C. M. (2017). Studies on the Vitamin C transporter gene SLC23A2 and cardiac conduction. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/58655 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:46543/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Tang, Joyce Chi Man. “Studies on the Vitamin C transporter gene SLC23A2 and cardiac conduction.” 2017. Masters Thesis, University of New South Wales. Accessed May 26, 2019. http://handle.unsw.edu.au/1959.4/58655 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:46543/SOURCE02?view=true.

MLA Handbook (7th Edition):

Tang, Joyce Chi Man. “Studies on the Vitamin C transporter gene SLC23A2 and cardiac conduction.” 2017. Web. 26 May 2019.

Vancouver:

Tang JCM. Studies on the Vitamin C transporter gene SLC23A2 and cardiac conduction. [Internet] [Masters thesis]. University of New South Wales; 2017. [cited 2019 May 26]. Available from: http://handle.unsw.edu.au/1959.4/58655 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:46543/SOURCE02?view=true.

Council of Science Editors:

Tang JCM. Studies on the Vitamin C transporter gene SLC23A2 and cardiac conduction. [Masters Thesis]. University of New South Wales; 2017. Available from: http://handle.unsw.edu.au/1959.4/58655 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:46543/SOURCE02?view=true


University of Illinois – Chicago

13. Obando, Julio E. Assessment of the Clinical Validity and Utility of SNPs When Used as Predictors for Periodontitis.

Degree: 2017, University of Illinois – Chicago

 BACKGROUND Chronic periodontitis is an inflammatory disease, influenced by a multifactorial etiology; susceptible host, environmental factors, microbial colonization and genetic variations. As genes determine qualitative… (more)

Subjects/Keywords: periodontitis; polymorphisms; genetics; single nucleotide polymorphisms; genetic testing

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APA (6th Edition):

Obando, J. E. (2017). Assessment of the Clinical Validity and Utility of SNPs When Used as Predictors for Periodontitis. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/21820

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):

Obando, Julio E. “Assessment of the Clinical Validity and Utility of SNPs When Used as Predictors for Periodontitis.” 2017. Thesis, University of Illinois – Chicago. Accessed May 26, 2019. http://hdl.handle.net/10027/21820.

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

MLA Handbook (7th Edition):

Obando, Julio E. “Assessment of the Clinical Validity and Utility of SNPs When Used as Predictors for Periodontitis.” 2017. Web. 26 May 2019.

Vancouver:

Obando JE. Assessment of the Clinical Validity and Utility of SNPs When Used as Predictors for Periodontitis. [Internet] [Thesis]. University of Illinois – Chicago; 2017. [cited 2019 May 26]. Available from: http://hdl.handle.net/10027/21820.

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

Council of Science Editors:

Obando JE. Assessment of the Clinical Validity and Utility of SNPs When Used as Predictors for Periodontitis. [Thesis]. University of Illinois – Chicago; 2017. Available from: http://hdl.handle.net/10027/21820

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


Durban University of Technology

14. Makamure, Michelle. A genetic epidemiological study of prevalence and association of genetic polymorphisms in asthma related phenotypes among children in Durban, Kwazulu-Natal.

Degree: 2012, Durban University of Technology

Submitted in fulfillment of the requirements for the degree of Master of Technology: Health Sciences, Durban University of Technology, Durban, South Africa, 2013.

Several genes… (more)

Subjects/Keywords: Genetic polymorphisms; Asthma in children; Respiratory allergy

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APA (6th Edition):

Makamure, M. (2012). A genetic epidemiological study of prevalence and association of genetic polymorphisms in asthma related phenotypes among children in Durban, Kwazulu-Natal. (Thesis). Durban University of Technology. Retrieved from http://hdl.handle.net/10321/2980

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):

Makamure, Michelle. “A genetic epidemiological study of prevalence and association of genetic polymorphisms in asthma related phenotypes among children in Durban, Kwazulu-Natal.” 2012. Thesis, Durban University of Technology. Accessed May 26, 2019. http://hdl.handle.net/10321/2980.

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

MLA Handbook (7th Edition):

Makamure, Michelle. “A genetic epidemiological study of prevalence and association of genetic polymorphisms in asthma related phenotypes among children in Durban, Kwazulu-Natal.” 2012. Web. 26 May 2019.

Vancouver:

Makamure M. A genetic epidemiological study of prevalence and association of genetic polymorphisms in asthma related phenotypes among children in Durban, Kwazulu-Natal. [Internet] [Thesis]. Durban University of Technology; 2012. [cited 2019 May 26]. Available from: http://hdl.handle.net/10321/2980.

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

Council of Science Editors:

Makamure M. A genetic epidemiological study of prevalence and association of genetic polymorphisms in asthma related phenotypes among children in Durban, Kwazulu-Natal. [Thesis]. Durban University of Technology; 2012. Available from: http://hdl.handle.net/10321/2980

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


University of Utah

15. Carr, Brian Allen. Function and regulation of pulmonary expressed cytochrome P450 enzymes;.

Degree: PhD, Pharmacology & Toxicology;, 2003, University of Utah

 Humans are exposed to a variety of inhaled and systemic xenobiotic compounds that cause respiratory toxicity. Cytochrome P450 enzymes, expressed specifically in lung tissues, are… (more)

Subjects/Keywords: Xenobiotic; Metabolism; Polymorphisms

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APA (6th Edition):

Carr, B. A. (2003). Function and regulation of pulmonary expressed cytochrome P450 enzymes;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/715/rec/546

Chicago Manual of Style (16th Edition):

Carr, Brian Allen. “Function and regulation of pulmonary expressed cytochrome P450 enzymes;.” 2003. Doctoral Dissertation, University of Utah. Accessed May 26, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/715/rec/546.

MLA Handbook (7th Edition):

Carr, Brian Allen. “Function and regulation of pulmonary expressed cytochrome P450 enzymes;.” 2003. Web. 26 May 2019.

Vancouver:

Carr BA. Function and regulation of pulmonary expressed cytochrome P450 enzymes;. [Internet] [Doctoral dissertation]. University of Utah; 2003. [cited 2019 May 26]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/715/rec/546.

Council of Science Editors:

Carr BA. Function and regulation of pulmonary expressed cytochrome P450 enzymes;. [Doctoral Dissertation]. University of Utah; 2003. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/715/rec/546

16. Custódio, Aline Cadurin. Análise de polimorfismos em tumores gliais humanos.

Degree: PhD, Genética, 2011, University of São Paulo

Os tumores do sistema nervoso central representam aproximadamente 2% de todos os tipos de cânceres. Embora a incidência dos tumores do SNC seja pequena, comparada… (more)

Subjects/Keywords: Astrocitomas; Astrocytomas; Glioblastoma; Glioblastomas; Polimorfismo; Polymorphisms

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APA (6th Edition):

Custódio, A. C. (2011). Análise de polimorfismos em tumores gliais humanos. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/17/17135/tde-25052011-153254/ ;

Chicago Manual of Style (16th Edition):

Custódio, Aline Cadurin. “Análise de polimorfismos em tumores gliais humanos.” 2011. Doctoral Dissertation, University of São Paulo. Accessed May 26, 2019. http://www.teses.usp.br/teses/disponiveis/17/17135/tde-25052011-153254/ ;.

MLA Handbook (7th Edition):

Custódio, Aline Cadurin. “Análise de polimorfismos em tumores gliais humanos.” 2011. Web. 26 May 2019.

Vancouver:

Custódio AC. Análise de polimorfismos em tumores gliais humanos. [Internet] [Doctoral dissertation]. University of São Paulo; 2011. [cited 2019 May 26]. Available from: http://www.teses.usp.br/teses/disponiveis/17/17135/tde-25052011-153254/ ;.

Council of Science Editors:

Custódio AC. Análise de polimorfismos em tumores gliais humanos. [Doctoral Dissertation]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/17/17135/tde-25052011-153254/ ;


Universidade Estadual de Campinas

17. Isabel Cristina Jacinto de Faria. Polymorphisms in the TGFB1, CD14, IL4, IL4-Ra, e ADAM33 genes and asthma severity.

Degree: Faculdade de Ciências Médicas, 2007, Universidade Estadual de Campinas

A Asma é uma doença inflamatória crônica de vias aéreas, na qual várias células têm papel fundamental, tais como os eosinófilos, mastócitos e linfócitos T.… (more)

Subjects/Keywords: Genes; Gene; Polymorphisms; Asma; Polimorfismos (Genetica); Asthma

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

APA (6th Edition):

Faria, I. C. J. d. (2007). Polymorphisms in the TGFB1, CD14, IL4, IL4-Ra, e ADAM33 genes and asthma severity. (Thesis). Universidade Estadual de Campinas. Retrieved from http://libdigi.unicamp.br/document/?code=vtls000416073

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):

Faria, Isabel Cristina Jacinto de. “Polymorphisms in the TGFB1, CD14, IL4, IL4-Ra, e ADAM33 genes and asthma severity.” 2007. Thesis, Universidade Estadual de Campinas. Accessed May 26, 2019. http://libdigi.unicamp.br/document/?code=vtls000416073.

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

MLA Handbook (7th Edition):

Faria, Isabel Cristina Jacinto de. “Polymorphisms in the TGFB1, CD14, IL4, IL4-Ra, e ADAM33 genes and asthma severity.” 2007. Web. 26 May 2019.

Vancouver:

Faria ICJd. Polymorphisms in the TGFB1, CD14, IL4, IL4-Ra, e ADAM33 genes and asthma severity. [Internet] [Thesis]. Universidade Estadual de Campinas; 2007. [cited 2019 May 26]. Available from: http://libdigi.unicamp.br/document/?code=vtls000416073.

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

Council of Science Editors:

Faria ICJd. Polymorphisms in the TGFB1, CD14, IL4, IL4-Ra, e ADAM33 genes and asthma severity. [Thesis]. Universidade Estadual de Campinas; 2007. Available from: http://libdigi.unicamp.br/document/?code=vtls000416073

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


Universidade Estadual de Campinas

18. Ana Carolina Zimiani de Paiva. Associação dos polimorfismos Gln27, Glu27, Arg16 e Gly16 do gene ADRB2R com asma.

Degree: Faculdade de Ciências Médicas, 2007, Universidade Estadual de Campinas

The atopic asthma is an illness with 20% of average prevalence in the Brazilian population. It?s estimated that 60% of the asthma cases are intermittent… (more)

Subjects/Keywords: Asma; Asthma; Polimorfismos (Genetica); Polymorphisms (Genetic)

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

APA (6th Edition):

Paiva, A. C. Z. d. (2007). Associação dos polimorfismos Gln27, Glu27, Arg16 e Gly16 do gene ADRB2R com asma. (Thesis). Universidade Estadual de Campinas. Retrieved from http://libdigi.unicamp.br/document/?code=vtls000417683

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):

Paiva, Ana Carolina Zimiani de. “Associação dos polimorfismos Gln27, Glu27, Arg16 e Gly16 do gene ADRB2R com asma.” 2007. Thesis, Universidade Estadual de Campinas. Accessed May 26, 2019. http://libdigi.unicamp.br/document/?code=vtls000417683.

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

MLA Handbook (7th Edition):

Paiva, Ana Carolina Zimiani de. “Associação dos polimorfismos Gln27, Glu27, Arg16 e Gly16 do gene ADRB2R com asma.” 2007. Web. 26 May 2019.

Vancouver:

Paiva ACZd. Associação dos polimorfismos Gln27, Glu27, Arg16 e Gly16 do gene ADRB2R com asma. [Internet] [Thesis]. Universidade Estadual de Campinas; 2007. [cited 2019 May 26]. Available from: http://libdigi.unicamp.br/document/?code=vtls000417683.

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

Council of Science Editors:

Paiva ACZd. Associação dos polimorfismos Gln27, Glu27, Arg16 e Gly16 do gene ADRB2R com asma. [Thesis]. Universidade Estadual de Campinas; 2007. Available from: http://libdigi.unicamp.br/document/?code=vtls000417683

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

19. Fragkioudaki, Sofia. Διερεύνηση συμβολής κλινικοεργαστηριακών και γενετικών παραγόντων στη λεμφωματογένεση στο σύνδρομο Sjogren.

Degree: 2017, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

The heightened risk of non-Hodgkin lymphoma (NHL) development in primary Sjogren syndrome (SS) is well established. Several adverse clinical and laboratory predictors have been described.… (more)

Subjects/Keywords: Λέμφωμα; Μεθυλίωση; Πολυμορφισμοί; Lymphoma; Methylation; Polymorphisms

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

APA (6th Edition):

Fragkioudaki, S. (2017). Διερεύνηση συμβολής κλινικοεργαστηριακών και γενετικών παραγόντων στη λεμφωματογένεση στο σύνδρομο Sjogren. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/42170

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):

Fragkioudaki, Sofia. “Διερεύνηση συμβολής κλινικοεργαστηριακών και γενετικών παραγόντων στη λεμφωματογένεση στο σύνδρομο Sjogren.” 2017. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed May 26, 2019. http://hdl.handle.net/10442/hedi/42170.

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

MLA Handbook (7th Edition):

Fragkioudaki, Sofia. “Διερεύνηση συμβολής κλινικοεργαστηριακών και γενετικών παραγόντων στη λεμφωματογένεση στο σύνδρομο Sjogren.” 2017. Web. 26 May 2019.

Vancouver:

Fragkioudaki S. Διερεύνηση συμβολής κλινικοεργαστηριακών και γενετικών παραγόντων στη λεμφωματογένεση στο σύνδρομο Sjogren. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2017. [cited 2019 May 26]. Available from: http://hdl.handle.net/10442/hedi/42170.

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

Council of Science Editors:

Fragkioudaki S. Διερεύνηση συμβολής κλινικοεργαστηριακών και γενετικών παραγόντων στη λεμφωματογένεση στο σύνδρομο Sjogren. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2017. Available from: http://hdl.handle.net/10442/hedi/42170

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


Univerzitet u Beogradu

20. Ilić, Vesna M., 1965-. Uloga polimorfizama gena za angiotenzinogen, angiotenzin-konvertujući enzim i AT1 receptor u razvoju nefropatije u dijabetesu tipa I.

Degree: Biološki fakultet, 2015, Univerzitet u Beogradu

Biologija - Genetika / Biology - Genetics

Dijabetesna nefropatija (DN) je jedna od najozbiljnijih mikrovaskularnih komplikacija, kako u tipu I, tako i u tipu II dijabetesa...

Advisors/Committee Members: Cvetković, Dragana, 1961-.

Subjects/Keywords: diabetic nephropathy; renin-angiotensin system; gene polymorphisms

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APA (6th Edition):

Ilić, Vesna M., 1. (2015). Uloga polimorfizama gena za angiotenzinogen, angiotenzin-konvertujući enzim i AT1 receptor u razvoju nefropatije u dijabetesu tipa I. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:9144/bdef:Content/get

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):

Ilić, Vesna M., 1965-. “Uloga polimorfizama gena za angiotenzinogen, angiotenzin-konvertujući enzim i AT1 receptor u razvoju nefropatije u dijabetesu tipa I.” 2015. Thesis, Univerzitet u Beogradu. Accessed May 26, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:9144/bdef:Content/get.

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

MLA Handbook (7th Edition):

Ilić, Vesna M., 1965-. “Uloga polimorfizama gena za angiotenzinogen, angiotenzin-konvertujući enzim i AT1 receptor u razvoju nefropatije u dijabetesu tipa I.” 2015. Web. 26 May 2019.

Vancouver:

Ilić, Vesna M. 1. Uloga polimorfizama gena za angiotenzinogen, angiotenzin-konvertujući enzim i AT1 receptor u razvoju nefropatije u dijabetesu tipa I. [Internet] [Thesis]. Univerzitet u Beogradu; 2015. [cited 2019 May 26]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:9144/bdef:Content/get.

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

Council of Science Editors:

Ilić, Vesna M. 1. Uloga polimorfizama gena za angiotenzinogen, angiotenzin-konvertujući enzim i AT1 receptor u razvoju nefropatije u dijabetesu tipa I. [Thesis]. Univerzitet u Beogradu; 2015. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:9144/bdef:Content/get

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


Univerzitet u Beogradu

21. Popović-Kuzmanović, Dragana V. Analiza polimorfizama gena značajnih za diferencijaciju T(H)17 i T regulatornih ćelija kod bolesnika sa antifosfolipidnim sindromom.

Degree: Medicinski fakultet, 2015, Univerzitet u Beogradu

 Uvod: Antifosfolipidni sindrom (AFS) je autoimunska bolest koju karakteri#e pojava arterijskih i venskih tromboza, gubitak ploda i prisustvo antifosfolipidnih antitela u serumu. AFS, kao i… (more)

Subjects/Keywords: Th17; Treg; Antiphospholipid syndrome; gene polymorphisms

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APA (6th Edition):

Popović-Kuzmanović, D. V. (2015). Analiza polimorfizama gena značajnih za diferencijaciju T(H)17 i T regulatornih ćelija kod bolesnika sa antifosfolipidnim sindromom. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:9848/bdef:Content/get

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):

Popović-Kuzmanović, Dragana V. “Analiza polimorfizama gena značajnih za diferencijaciju T(H)17 i T regulatornih ćelija kod bolesnika sa antifosfolipidnim sindromom.” 2015. Thesis, Univerzitet u Beogradu. Accessed May 26, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:9848/bdef:Content/get.

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

MLA Handbook (7th Edition):

Popović-Kuzmanović, Dragana V. “Analiza polimorfizama gena značajnih za diferencijaciju T(H)17 i T regulatornih ćelija kod bolesnika sa antifosfolipidnim sindromom.” 2015. Web. 26 May 2019.

Vancouver:

Popović-Kuzmanović DV. Analiza polimorfizama gena značajnih za diferencijaciju T(H)17 i T regulatornih ćelija kod bolesnika sa antifosfolipidnim sindromom. [Internet] [Thesis]. Univerzitet u Beogradu; 2015. [cited 2019 May 26]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:9848/bdef:Content/get.

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

Council of Science Editors:

Popović-Kuzmanović DV. Analiza polimorfizama gena značajnih za diferencijaciju T(H)17 i T regulatornih ćelija kod bolesnika sa antifosfolipidnim sindromom. [Thesis]. Univerzitet u Beogradu; 2015. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:9848/bdef:Content/get

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


Dublin City University

22. Minguzzi, Stefano. Investigation of the human folate gene MTHFD1L: polymorphisms and disease risk.

Degree: School of Biotechnology, 2013, Dublin City University

 The MTHFD1L gene encodes the mitochondrial monofunctional enzyme with proven 10-formyltetrahydrofolate synthetase activity. MTHFD1L expression is upregulated in human colon cancer and breast cancer, and… (more)

Subjects/Keywords: Biotechnology; Folate MTHFD1L polymorphisms cleft miRNA NTD

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APA (6th Edition):

Minguzzi, S. (2013). Investigation of the human folate gene MTHFD1L: polymorphisms and disease risk. (Thesis). Dublin City University. Retrieved from http://doras.dcu.ie/19391/

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):

Minguzzi, Stefano. “Investigation of the human folate gene MTHFD1L: polymorphisms and disease risk.” 2013. Thesis, Dublin City University. Accessed May 26, 2019. http://doras.dcu.ie/19391/.

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

MLA Handbook (7th Edition):

Minguzzi, Stefano. “Investigation of the human folate gene MTHFD1L: polymorphisms and disease risk.” 2013. Web. 26 May 2019.

Vancouver:

Minguzzi S. Investigation of the human folate gene MTHFD1L: polymorphisms and disease risk. [Internet] [Thesis]. Dublin City University; 2013. [cited 2019 May 26]. Available from: http://doras.dcu.ie/19391/.

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

Council of Science Editors:

Minguzzi S. Investigation of the human folate gene MTHFD1L: polymorphisms and disease risk. [Thesis]. Dublin City University; 2013. Available from: http://doras.dcu.ie/19391/

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


Hong Kong University of Science and Technology

23. Yang, Guangyuan. Permutation tests for genome-wide association studies.

Degree: 2014, Hong Kong University of Science and Technology

 In genome wide association studies (GWAS), there are single-nucleotide polymorphism (SNP) pairs which have significant associations with diseases via the combination of their main effects… (more)

Subjects/Keywords: Single nucleotide polymorphisms; Testing; Data processing

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APA (6th Edition):

Yang, G. (2014). Permutation tests for genome-wide association studies. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1432208 ; http://repository.ust.hk/ir/bitstream/1783.1-88026/1/th_redirect.html

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):

Yang, Guangyuan. “Permutation tests for genome-wide association studies.” 2014. Thesis, Hong Kong University of Science and Technology. Accessed May 26, 2019. https://doi.org/10.14711/thesis-b1432208 ; http://repository.ust.hk/ir/bitstream/1783.1-88026/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Yang, Guangyuan. “Permutation tests for genome-wide association studies.” 2014. Web. 26 May 2019.

Vancouver:

Yang G. Permutation tests for genome-wide association studies. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2019 May 26]. Available from: https://doi.org/10.14711/thesis-b1432208 ; http://repository.ust.hk/ir/bitstream/1783.1-88026/1/th_redirect.html.

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

Council of Science Editors:

Yang G. Permutation tests for genome-wide association studies. [Thesis]. Hong Kong University of Science and Technology; 2014. Available from: https://doi.org/10.14711/thesis-b1432208 ; http://repository.ust.hk/ir/bitstream/1783.1-88026/1/th_redirect.html

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


Hong Kong University of Science and Technology

24. Pun, Wing Frank. Imprinting in the schizophrenia-associated gene GABRB2 encoding GABAA̳ receptor ß₂ subunit.

Degree: 2010, Hong Kong University of Science and Technology

 Schizophrenia is a complex genetic disorder, the inheritance pattern of which is likely complicated by epigenetic factors yet to be elucidated. In the present study,… (more)

Subjects/Keywords: GABA  – Receptors; Schizophrenia  – Genetic aspects; Genetic polymorphisms

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APA (6th Edition):

Pun, W. F. (2010). Imprinting in the schizophrenia-associated gene GABRB2 encoding GABAA̳ receptor ß₂ subunit. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1097724 ; http://repository.ust.hk/ir/bitstream/1783.1-6459/1/th_redirect.html

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):

Pun, Wing Frank. “Imprinting in the schizophrenia-associated gene GABRB2 encoding GABAA̳ receptor ß₂ subunit.” 2010. Thesis, Hong Kong University of Science and Technology. Accessed May 26, 2019. https://doi.org/10.14711/thesis-b1097724 ; http://repository.ust.hk/ir/bitstream/1783.1-6459/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Pun, Wing Frank. “Imprinting in the schizophrenia-associated gene GABRB2 encoding GABAA̳ receptor ß₂ subunit.” 2010. Web. 26 May 2019.

Vancouver:

Pun WF. Imprinting in the schizophrenia-associated gene GABRB2 encoding GABAA̳ receptor ß₂ subunit. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2010. [cited 2019 May 26]. Available from: https://doi.org/10.14711/thesis-b1097724 ; http://repository.ust.hk/ir/bitstream/1783.1-6459/1/th_redirect.html.

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

Council of Science Editors:

Pun WF. Imprinting in the schizophrenia-associated gene GABRB2 encoding GABAA̳ receptor ß₂ subunit. [Thesis]. Hong Kong University of Science and Technology; 2010. Available from: https://doi.org/10.14711/thesis-b1097724 ; http://repository.ust.hk/ir/bitstream/1783.1-6459/1/th_redirect.html

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


University of Hong Kong

25. Man, On-ying. Serum amyloid A 1 (SAA1) polymorphisms are associated with variation in tumor suppressive activities in esophageal squamous cell carcinoma (ESCC).

Degree: PhD, 2015, University of Hong Kong

Esophageal cancer (EC), a malignancy originated from the epithelium of the esophagus, ranks eighth in incidence rate of cancer, sixth as the most common cause… (more)

Subjects/Keywords: Genetic polymorphisms; Antioncogenes; Esophagus - Cancer - Genetic aspects

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APA (6th Edition):

Man, O. (2015). Serum amyloid A 1 (SAA1) polymorphisms are associated with variation in tumor suppressive activities in esophageal squamous cell carcinoma (ESCC). (Doctoral Dissertation). University of Hong Kong. Retrieved from Man, O. [萬安瑩]. (2015). Serum amyloid A 1 (SAA1) polymorphisms are associated with variation in tumor suppressive activities in esophageal squamous cell carcinoma (ESCC). (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5558986 ; http://hdl.handle.net/10722/216255

Chicago Manual of Style (16th Edition):

Man, On-ying. “Serum amyloid A 1 (SAA1) polymorphisms are associated with variation in tumor suppressive activities in esophageal squamous cell carcinoma (ESCC).” 2015. Doctoral Dissertation, University of Hong Kong. Accessed May 26, 2019. Man, O. [萬安瑩]. (2015). Serum amyloid A 1 (SAA1) polymorphisms are associated with variation in tumor suppressive activities in esophageal squamous cell carcinoma (ESCC). (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5558986 ; http://hdl.handle.net/10722/216255.

MLA Handbook (7th Edition):

Man, On-ying. “Serum amyloid A 1 (SAA1) polymorphisms are associated with variation in tumor suppressive activities in esophageal squamous cell carcinoma (ESCC).” 2015. Web. 26 May 2019.

Vancouver:

Man O. Serum amyloid A 1 (SAA1) polymorphisms are associated with variation in tumor suppressive activities in esophageal squamous cell carcinoma (ESCC). [Internet] [Doctoral dissertation]. University of Hong Kong; 2015. [cited 2019 May 26]. Available from: Man, O. [萬安瑩]. (2015). Serum amyloid A 1 (SAA1) polymorphisms are associated with variation in tumor suppressive activities in esophageal squamous cell carcinoma (ESCC). (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5558986 ; http://hdl.handle.net/10722/216255.

Council of Science Editors:

Man O. Serum amyloid A 1 (SAA1) polymorphisms are associated with variation in tumor suppressive activities in esophageal squamous cell carcinoma (ESCC). [Doctoral Dissertation]. University of Hong Kong; 2015. Available from: Man, O. [萬安瑩]. (2015). Serum amyloid A 1 (SAA1) polymorphisms are associated with variation in tumor suppressive activities in esophageal squamous cell carcinoma (ESCC). (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5558986 ; http://hdl.handle.net/10722/216255


University of Louisville

26. Leggett, Carmine Simone. Functional effects of CYP1A2, NAT1, and NAT2 genetic variants in nucleotide excision repair-deficient human fibroblasts : implications for toxicological risk from environmental arylamines.

Degree: MS, 2010, University of Louisville

 Arylamine N-acetyltransferase 1 (NAT1) and 2 (NAT2) catalyze the detoxification and/or activation of aromatic and heterocyclic amine carcinogens by two pathways. This metabolism reaction can… (more)

Subjects/Keywords: N-acetyltransferase; Arylamines; Single nucleotide polymorphisms (SNPs)

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APA (6th Edition):

Leggett, C. S. (2010). Functional effects of CYP1A2, NAT1, and NAT2 genetic variants in nucleotide excision repair-deficient human fibroblasts : implications for toxicological risk from environmental arylamines. (Masters Thesis). University of Louisville. Retrieved from 10.18297/etd/811 ; https://ir.library.louisville.edu/etd/811

Chicago Manual of Style (16th Edition):

Leggett, Carmine Simone. “Functional effects of CYP1A2, NAT1, and NAT2 genetic variants in nucleotide excision repair-deficient human fibroblasts : implications for toxicological risk from environmental arylamines.” 2010. Masters Thesis, University of Louisville. Accessed May 26, 2019. 10.18297/etd/811 ; https://ir.library.louisville.edu/etd/811.

MLA Handbook (7th Edition):

Leggett, Carmine Simone. “Functional effects of CYP1A2, NAT1, and NAT2 genetic variants in nucleotide excision repair-deficient human fibroblasts : implications for toxicological risk from environmental arylamines.” 2010. Web. 26 May 2019.

Vancouver:

Leggett CS. Functional effects of CYP1A2, NAT1, and NAT2 genetic variants in nucleotide excision repair-deficient human fibroblasts : implications for toxicological risk from environmental arylamines. [Internet] [Masters thesis]. University of Louisville; 2010. [cited 2019 May 26]. Available from: 10.18297/etd/811 ; https://ir.library.louisville.edu/etd/811.

Council of Science Editors:

Leggett CS. Functional effects of CYP1A2, NAT1, and NAT2 genetic variants in nucleotide excision repair-deficient human fibroblasts : implications for toxicological risk from environmental arylamines. [Masters Thesis]. University of Louisville; 2010. Available from: 10.18297/etd/811 ; https://ir.library.louisville.edu/etd/811


Penn State University

27. Nichenametla, Sailendra Nath. FUNCTIONAL SIGNIFICANCE OF THE GAG TRINUCLEOTIDE-REPEAT POLYMORPHISM IN THE CATALYTIC SUBUNIT OF THE GLUTATHIONE BIOSYNTHETIC ENZYME, g-GLUTAMYLCYSTEINE LIGASE.

Degree: PhD, Integrative Biosciences, 2010, Penn State University

 Glutathione (GSH), the most abundant intracellular antioxidant, is proposed to prevent cancer through multiple biochemical pathways including carcinogen detoxification, scavenging and neutralizing free radicals, modulating… (more)

Subjects/Keywords: cancer; trinucleotide repeat polymorphisms; Oxidative stress; glutathione

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APA (6th Edition):

Nichenametla, S. N. (2010). FUNCTIONAL SIGNIFICANCE OF THE GAG TRINUCLEOTIDE-REPEAT POLYMORPHISM IN THE CATALYTIC SUBUNIT OF THE GLUTATHIONE BIOSYNTHETIC ENZYME, g-GLUTAMYLCYSTEINE LIGASE. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/11100

Chicago Manual of Style (16th Edition):

Nichenametla, Sailendra Nath. “FUNCTIONAL SIGNIFICANCE OF THE GAG TRINUCLEOTIDE-REPEAT POLYMORPHISM IN THE CATALYTIC SUBUNIT OF THE GLUTATHIONE BIOSYNTHETIC ENZYME, g-GLUTAMYLCYSTEINE LIGASE.” 2010. Doctoral Dissertation, Penn State University. Accessed May 26, 2019. https://etda.libraries.psu.edu/catalog/11100.

MLA Handbook (7th Edition):

Nichenametla, Sailendra Nath. “FUNCTIONAL SIGNIFICANCE OF THE GAG TRINUCLEOTIDE-REPEAT POLYMORPHISM IN THE CATALYTIC SUBUNIT OF THE GLUTATHIONE BIOSYNTHETIC ENZYME, g-GLUTAMYLCYSTEINE LIGASE.” 2010. Web. 26 May 2019.

Vancouver:

Nichenametla SN. FUNCTIONAL SIGNIFICANCE OF THE GAG TRINUCLEOTIDE-REPEAT POLYMORPHISM IN THE CATALYTIC SUBUNIT OF THE GLUTATHIONE BIOSYNTHETIC ENZYME, g-GLUTAMYLCYSTEINE LIGASE. [Internet] [Doctoral dissertation]. Penn State University; 2010. [cited 2019 May 26]. Available from: https://etda.libraries.psu.edu/catalog/11100.

Council of Science Editors:

Nichenametla SN. FUNCTIONAL SIGNIFICANCE OF THE GAG TRINUCLEOTIDE-REPEAT POLYMORPHISM IN THE CATALYTIC SUBUNIT OF THE GLUTATHIONE BIOSYNTHETIC ENZYME, g-GLUTAMYLCYSTEINE LIGASE. [Doctoral Dissertation]. Penn State University; 2010. Available from: https://etda.libraries.psu.edu/catalog/11100


University of Manchester

28. Dhaygude, Ajay. Epidemiology, genetic differences and clinical outcomes of antineutrophil cytoplasmic autoantibody associated systemic vasculitis.

Degree: Thesis (M.D.), 2012, University of Manchester

 Introduction: The two subtypes of Antineutrophil Cytoplasmic autoantibody associated systemic vasculitis (AASV) cANCA and pANCA associated vasculitis are the commonest causes of rapidly progressive glomerulonephritis.… (more)

Subjects/Keywords: 616.07; ANCA, vasculitis, epidemiology, cytokine, polymorphisms, metabolomics

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APA (6th Edition):

Dhaygude, A. (2012). Epidemiology, genetic differences and clinical outcomes of antineutrophil cytoplasmic autoantibody associated systemic vasculitis. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/epidemiology-genetic-differencesand-clinical-outcomes-ofantineutrophil-cytoplasmicautoantibody-associated-systemicvasculitis(1d4bf70b-3046-4997-9bdb-82206b6a8264).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.549027

Chicago Manual of Style (16th Edition):

Dhaygude, Ajay. “Epidemiology, genetic differences and clinical outcomes of antineutrophil cytoplasmic autoantibody associated systemic vasculitis.” 2012. Doctoral Dissertation, University of Manchester. Accessed May 26, 2019. https://www.research.manchester.ac.uk/portal/en/theses/epidemiology-genetic-differencesand-clinical-outcomes-ofantineutrophil-cytoplasmicautoantibody-associated-systemicvasculitis(1d4bf70b-3046-4997-9bdb-82206b6a8264).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.549027.

MLA Handbook (7th Edition):

Dhaygude, Ajay. “Epidemiology, genetic differences and clinical outcomes of antineutrophil cytoplasmic autoantibody associated systemic vasculitis.” 2012. Web. 26 May 2019.

Vancouver:

Dhaygude A. Epidemiology, genetic differences and clinical outcomes of antineutrophil cytoplasmic autoantibody associated systemic vasculitis. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2019 May 26]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/epidemiology-genetic-differencesand-clinical-outcomes-ofantineutrophil-cytoplasmicautoantibody-associated-systemicvasculitis(1d4bf70b-3046-4997-9bdb-82206b6a8264).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.549027.

Council of Science Editors:

Dhaygude A. Epidemiology, genetic differences and clinical outcomes of antineutrophil cytoplasmic autoantibody associated systemic vasculitis. [Doctoral Dissertation]. University of Manchester; 2012. Available from: https://www.research.manchester.ac.uk/portal/en/theses/epidemiology-genetic-differencesand-clinical-outcomes-ofantineutrophil-cytoplasmicautoantibody-associated-systemicvasculitis(1d4bf70b-3046-4997-9bdb-82206b6a8264).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.549027


University of Florida

29. El Rouby, Nihal M. Identification of Genetic Predictors of Resistant Hypertension through Genome Wide Association Analysis Coupled with Induced Pluripotent Stem Cells.

Degree: PhD, Pharmaceutical Sciences - Pharmacotherapy and Translational Research, 2017, University of Florida

Subjects/Keywords: bloodpressure; polymorphisms; resistanthypertension

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

APA (6th Edition):

El Rouby, N. M. (2017). Identification of Genetic Predictors of Resistant Hypertension through Genome Wide Association Analysis Coupled with Induced Pluripotent Stem Cells. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0050967

Chicago Manual of Style (16th Edition):

El Rouby, Nihal M. “Identification of Genetic Predictors of Resistant Hypertension through Genome Wide Association Analysis Coupled with Induced Pluripotent Stem Cells.” 2017. Doctoral Dissertation, University of Florida. Accessed May 26, 2019. http://ufdc.ufl.edu/UFE0050967.

MLA Handbook (7th Edition):

El Rouby, Nihal M. “Identification of Genetic Predictors of Resistant Hypertension through Genome Wide Association Analysis Coupled with Induced Pluripotent Stem Cells.” 2017. Web. 26 May 2019.

Vancouver:

El Rouby NM. Identification of Genetic Predictors of Resistant Hypertension through Genome Wide Association Analysis Coupled with Induced Pluripotent Stem Cells. [Internet] [Doctoral dissertation]. University of Florida; 2017. [cited 2019 May 26]. Available from: http://ufdc.ufl.edu/UFE0050967.

Council of Science Editors:

El Rouby NM. Identification of Genetic Predictors of Resistant Hypertension through Genome Wide Association Analysis Coupled with Induced Pluripotent Stem Cells. [Doctoral Dissertation]. University of Florida; 2017. Available from: http://ufdc.ufl.edu/UFE0050967


University of the Western Cape

30. October, Firzana. Proteomic and SNP analysis of the Cadherin 10 type-II (CDH10) gene, in the South African autistic population .

Degree: 2013, University of the Western Cape

 Autism or autism spectrum disorder (ASD) is a very diverse neurological disorder that manifests specifically in children and infants between the ages of two to… (more)

Subjects/Keywords: Autism; Biomarkers; Mass spectrometry; Single nucleotide polymorphisms

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APA (6th Edition):

October, F. (2013). Proteomic and SNP analysis of the Cadherin 10 type-II (CDH10) gene, in the South African autistic population . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/4826

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):

October, Firzana. “Proteomic and SNP analysis of the Cadherin 10 type-II (CDH10) gene, in the South African autistic population .” 2013. Thesis, University of the Western Cape. Accessed May 26, 2019. http://hdl.handle.net/11394/4826.

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

MLA Handbook (7th Edition):

October, Firzana. “Proteomic and SNP analysis of the Cadherin 10 type-II (CDH10) gene, in the South African autistic population .” 2013. Web. 26 May 2019.

Vancouver:

October F. Proteomic and SNP analysis of the Cadherin 10 type-II (CDH10) gene, in the South African autistic population . [Internet] [Thesis]. University of the Western Cape; 2013. [cited 2019 May 26]. Available from: http://hdl.handle.net/11394/4826.

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

Council of Science Editors:

October F. Proteomic and SNP analysis of the Cadherin 10 type-II (CDH10) gene, in the South African autistic population . [Thesis]. University of the Western Cape; 2013. Available from: http://hdl.handle.net/11394/4826

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

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