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You searched for subject:(Genetic). Showing records 1 – 30 of 13903 total matches.

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University of Helsinki

1. Andersen, Mette. The grey zone between type 1 and type 2 diabetes : genetic aspects of diabetes in adults.

Degree: Institute of Clinical Medicine; Folkhälsan Research Center, 2012, University of Helsinki

In the last decades the prevalence of diabetes has increased dramatically. Diabetes is a complex disease often subdivided into type 1 diabetes, characterized by autoimmune… (more)

Subjects/Keywords: genetic epidemiology; genetic epidemiology

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APA (6th Edition):

Andersen, M. (2012). The grey zone between type 1 and type 2 diabetes : genetic aspects of diabetes in adults. (Doctoral Dissertation). University of Helsinki. Retrieved from http://hdl.handle.net/10138/37472

Chicago Manual of Style (16th Edition):

Andersen, Mette. “The grey zone between type 1 and type 2 diabetes : genetic aspects of diabetes in adults.” 2012. Doctoral Dissertation, University of Helsinki. Accessed March 28, 2020. http://hdl.handle.net/10138/37472.

MLA Handbook (7th Edition):

Andersen, Mette. “The grey zone between type 1 and type 2 diabetes : genetic aspects of diabetes in adults.” 2012. Web. 28 Mar 2020.

Vancouver:

Andersen M. The grey zone between type 1 and type 2 diabetes : genetic aspects of diabetes in adults. [Internet] [Doctoral dissertation]. University of Helsinki; 2012. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10138/37472.

Council of Science Editors:

Andersen M. The grey zone between type 1 and type 2 diabetes : genetic aspects of diabetes in adults. [Doctoral Dissertation]. University of Helsinki; 2012. Available from: http://hdl.handle.net/10138/37472


Rutgers University

2. Bosacchi, Massimo, 1978-. The development of genetic markers for plastid transformation in higher plants.

Degree: PhD, Plant Biology, 2016, Rutgers University

The four studies that comprise my dissertation were undertaken in an effort to develop new selectable marker systems and expression elements that could make chloroplast… (more)

Subjects/Keywords: Plant genetic engineering; Genetic transformation

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APA (6th Edition):

Bosacchi, Massimo, 1. (2016). The development of genetic markers for plastid transformation in higher plants. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/51236/

Chicago Manual of Style (16th Edition):

Bosacchi, Massimo, 1978-. “The development of genetic markers for plastid transformation in higher plants.” 2016. Doctoral Dissertation, Rutgers University. Accessed March 28, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/51236/.

MLA Handbook (7th Edition):

Bosacchi, Massimo, 1978-. “The development of genetic markers for plastid transformation in higher plants.” 2016. Web. 28 Mar 2020.

Vancouver:

Bosacchi, Massimo 1. The development of genetic markers for plastid transformation in higher plants. [Internet] [Doctoral dissertation]. Rutgers University; 2016. [cited 2020 Mar 28]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/51236/.

Council of Science Editors:

Bosacchi, Massimo 1. The development of genetic markers for plastid transformation in higher plants. [Doctoral Dissertation]. Rutgers University; 2016. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/51236/


University of Georgia

3. Tang, Xiaojia. Computational systems biology for the biological clock of Neurospora crassa.

Degree: PhD, Physics, 2009, University of Georgia

Genetic networks have been applied to describe biological systems, e.g., the biological clock, from a systems biology perspective. A model-driven discovery process, Computing Life, is… (more)

Subjects/Keywords: genetic networks

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APA (6th Edition):

Tang, X. (2009). Computational systems biology for the biological clock of Neurospora crassa. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/tang_xiaojia_200908_phd

Chicago Manual of Style (16th Edition):

Tang, Xiaojia. “Computational systems biology for the biological clock of Neurospora crassa.” 2009. Doctoral Dissertation, University of Georgia. Accessed March 28, 2020. http://purl.galileo.usg.edu/uga_etd/tang_xiaojia_200908_phd.

MLA Handbook (7th Edition):

Tang, Xiaojia. “Computational systems biology for the biological clock of Neurospora crassa.” 2009. Web. 28 Mar 2020.

Vancouver:

Tang X. Computational systems biology for the biological clock of Neurospora crassa. [Internet] [Doctoral dissertation]. University of Georgia; 2009. [cited 2020 Mar 28]. Available from: http://purl.galileo.usg.edu/uga_etd/tang_xiaojia_200908_phd.

Council of Science Editors:

Tang X. Computational systems biology for the biological clock of Neurospora crassa. [Doctoral Dissertation]. University of Georgia; 2009. Available from: http://purl.galileo.usg.edu/uga_etd/tang_xiaojia_200908_phd


University of Georgia

4. Ujjwal, Kumar. Cyber haggler: web based bargaining using genetic algorithm.

Degree: MS, Artificial Intelligence, 2007, University of Georgia

 In this thesis, we analyze the sequential bargaining problem from a different perspective. Instead of taking a game theoretic approach, we model bargaining as a… (more)

Subjects/Keywords: Genetic Algorithm

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APA (6th Edition):

Ujjwal, K. (2007). Cyber haggler: web based bargaining using genetic algorithm. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/ujjwal_kumar_200705_ms

Chicago Manual of Style (16th Edition):

Ujjwal, Kumar. “Cyber haggler: web based bargaining using genetic algorithm.” 2007. Masters Thesis, University of Georgia. Accessed March 28, 2020. http://purl.galileo.usg.edu/uga_etd/ujjwal_kumar_200705_ms.

MLA Handbook (7th Edition):

Ujjwal, Kumar. “Cyber haggler: web based bargaining using genetic algorithm.” 2007. Web. 28 Mar 2020.

Vancouver:

Ujjwal K. Cyber haggler: web based bargaining using genetic algorithm. [Internet] [Masters thesis]. University of Georgia; 2007. [cited 2020 Mar 28]. Available from: http://purl.galileo.usg.edu/uga_etd/ujjwal_kumar_200705_ms.

Council of Science Editors:

Ujjwal K. Cyber haggler: web based bargaining using genetic algorithm. [Masters Thesis]. University of Georgia; 2007. Available from: http://purl.galileo.usg.edu/uga_etd/ujjwal_kumar_200705_ms


University of Hong Kong

5. Wong, Ka-mei. Validation of a translated Chinese perceived personal control (PPC) questionnaire in prenatal team-based genetic counselling.

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

Genetic counselling is an important component in a clinical genetic service, providing information to patients and assisting them in making decisions on reproduction and genetic(more)

Subjects/Keywords: Genetic counseling

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APA (6th Edition):

Wong, K. (2017). Validation of a translated Chinese perceived personal control (PPC) questionnaire in prenatal team-based genetic counselling. (Masters Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/251316

Chicago Manual of Style (16th Edition):

Wong, Ka-mei. “Validation of a translated Chinese perceived personal control (PPC) questionnaire in prenatal team-based genetic counselling.” 2017. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. http://hdl.handle.net/10722/251316.

MLA Handbook (7th Edition):

Wong, Ka-mei. “Validation of a translated Chinese perceived personal control (PPC) questionnaire in prenatal team-based genetic counselling.” 2017. Web. 28 Mar 2020.

Vancouver:

Wong K. Validation of a translated Chinese perceived personal control (PPC) questionnaire in prenatal team-based genetic counselling. [Internet] [Masters thesis]. University of Hong Kong; 2017. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10722/251316.

Council of Science Editors:

Wong K. Validation of a translated Chinese perceived personal control (PPC) questionnaire in prenatal team-based genetic counselling. [Masters Thesis]. University of Hong Kong; 2017. Available from: http://hdl.handle.net/10722/251316


University of Hong Kong

6. Ying, Dingge. Identification of shared extended haplotypes in both population-based studies of complex disease and family-based studies of Mendelian disorders.

Degree: PhD, 2013, University of Hong Kong

 Recent founder mutations may play important roles in complex diseases and Mendelian disorders. Detecting shared haplotypes of identity by descent (IBD) could facilitate discovery of… (more)

Subjects/Keywords: Genetic disorders

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APA (6th Edition):

Ying, D. (2013). Identification of shared extended haplotypes in both population-based studies of complex disease and family-based studies of Mendelian disorders. (Doctoral Dissertation). University of Hong Kong. Retrieved from Ying, D. [应鼎阁]. (2013). Identification of shared extended haplotypes in both population-based studies of complex disease and family-based studies of Mendelian disorders. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5137968 ; http://dx.doi.org/10.5353/th_b5137968 ; http://hdl.handle.net/10722/205837

Chicago Manual of Style (16th Edition):

Ying, Dingge. “Identification of shared extended haplotypes in both population-based studies of complex disease and family-based studies of Mendelian disorders.” 2013. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Ying, D. [应鼎阁]. (2013). Identification of shared extended haplotypes in both population-based studies of complex disease and family-based studies of Mendelian disorders. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5137968 ; http://dx.doi.org/10.5353/th_b5137968 ; http://hdl.handle.net/10722/205837.

MLA Handbook (7th Edition):

Ying, Dingge. “Identification of shared extended haplotypes in both population-based studies of complex disease and family-based studies of Mendelian disorders.” 2013. Web. 28 Mar 2020.

Vancouver:

Ying D. Identification of shared extended haplotypes in both population-based studies of complex disease and family-based studies of Mendelian disorders. [Internet] [Doctoral dissertation]. University of Hong Kong; 2013. [cited 2020 Mar 28]. Available from: Ying, D. [应鼎阁]. (2013). Identification of shared extended haplotypes in both population-based studies of complex disease and family-based studies of Mendelian disorders. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5137968 ; http://dx.doi.org/10.5353/th_b5137968 ; http://hdl.handle.net/10722/205837.

Council of Science Editors:

Ying D. Identification of shared extended haplotypes in both population-based studies of complex disease and family-based studies of Mendelian disorders. [Doctoral Dissertation]. University of Hong Kong; 2013. Available from: Ying, D. [应鼎阁]. (2013). Identification of shared extended haplotypes in both population-based studies of complex disease and family-based studies of Mendelian disorders. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5137968 ; http://dx.doi.org/10.5353/th_b5137968 ; http://hdl.handle.net/10722/205837


University of Hong Kong

7. 张璐; Zhang, Lu. Identification and prioritization of single nucleotide variation for Mendelian disorders from whole exome sequencing data.

Degree: M. Phil., 2012, University of Hong Kong

With the completion of human genome sequencing project and the rapid development of sequencing technologies, our capacity in tackling with genetic and genomic changes that… (more)

Subjects/Keywords: Genetic disorders.

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APA (6th Edition):

张璐; Zhang, L. (2012). Identification and prioritization of single nucleotide variation for Mendelian disorders from whole exome sequencing data. (Masters Thesis). University of Hong Kong. Retrieved from Zhang, L. [张璐]. (2012). Identification and prioritization of single nucleotide variation for Mendelian disorders from whole exome sequencing data. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4852190 ; http://dx.doi.org/10.5353/th_b4852190 ; http://hdl.handle.net/10722/179999

Chicago Manual of Style (16th Edition):

张璐; Zhang, Lu. “Identification and prioritization of single nucleotide variation for Mendelian disorders from whole exome sequencing data.” 2012. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. Zhang, L. [张璐]. (2012). Identification and prioritization of single nucleotide variation for Mendelian disorders from whole exome sequencing data. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4852190 ; http://dx.doi.org/10.5353/th_b4852190 ; http://hdl.handle.net/10722/179999.

MLA Handbook (7th Edition):

张璐; Zhang, Lu. “Identification and prioritization of single nucleotide variation for Mendelian disorders from whole exome sequencing data.” 2012. Web. 28 Mar 2020.

Vancouver:

张璐; Zhang L. Identification and prioritization of single nucleotide variation for Mendelian disorders from whole exome sequencing data. [Internet] [Masters thesis]. University of Hong Kong; 2012. [cited 2020 Mar 28]. Available from: Zhang, L. [张璐]. (2012). Identification and prioritization of single nucleotide variation for Mendelian disorders from whole exome sequencing data. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4852190 ; http://dx.doi.org/10.5353/th_b4852190 ; http://hdl.handle.net/10722/179999.

Council of Science Editors:

张璐; Zhang L. Identification and prioritization of single nucleotide variation for Mendelian disorders from whole exome sequencing data. [Masters Thesis]. University of Hong Kong; 2012. Available from: Zhang, L. [张璐]. (2012). Identification and prioritization of single nucleotide variation for Mendelian disorders from whole exome sequencing data. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4852190 ; http://dx.doi.org/10.5353/th_b4852190 ; http://hdl.handle.net/10722/179999

8. Satishkumar, M V. Simultaneous scheduling of machines and Agvs using evolutionary optimization algorithms.

Degree: 2010, Jawaharlal Nehru Technological University

 High degree of flexibility and quick response times have become essential features of modern manufacturing systems where customers are demanding for a variety of products… (more)

Subjects/Keywords: Genetic Algorithms

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APA (6th Edition):

Satishkumar, M. V. (2010). Simultaneous scheduling of machines and Agvs using evolutionary optimization algorithms. (Thesis). Jawaharlal Nehru Technological University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/2255

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):

Satishkumar, M V. “Simultaneous scheduling of machines and Agvs using evolutionary optimization algorithms.” 2010. Thesis, Jawaharlal Nehru Technological University. Accessed March 28, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/2255.

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

MLA Handbook (7th Edition):

Satishkumar, M V. “Simultaneous scheduling of machines and Agvs using evolutionary optimization algorithms.” 2010. Web. 28 Mar 2020.

Vancouver:

Satishkumar MV. Simultaneous scheduling of machines and Agvs using evolutionary optimization algorithms. [Internet] [Thesis]. Jawaharlal Nehru Technological University; 2010. [cited 2020 Mar 28]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/2255.

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

Council of Science Editors:

Satishkumar MV. Simultaneous scheduling of machines and Agvs using evolutionary optimization algorithms. [Thesis]. Jawaharlal Nehru Technological University; 2010. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/2255

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


Victoria University of Wellington

9. Downey, Carlton. Explorations in Parallel Linear Genetic Programming.

Degree: 2011, Victoria University of Wellington

 Linear Genetic Programming (LGP) is a powerful problem-solving technique, but one with several significant weaknesses. LGP programs consist of a linear sequence of instructions, where… (more)

Subjects/Keywords: Genetic programming

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APA (6th Edition):

Downey, C. (2011). Explorations in Parallel Linear Genetic Programming. (Masters Thesis). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/2312

Chicago Manual of Style (16th Edition):

Downey, Carlton. “Explorations in Parallel Linear Genetic Programming.” 2011. Masters Thesis, Victoria University of Wellington. Accessed March 28, 2020. http://hdl.handle.net/10063/2312.

MLA Handbook (7th Edition):

Downey, Carlton. “Explorations in Parallel Linear Genetic Programming.” 2011. Web. 28 Mar 2020.

Vancouver:

Downey C. Explorations in Parallel Linear Genetic Programming. [Internet] [Masters thesis]. Victoria University of Wellington; 2011. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10063/2312.

Council of Science Editors:

Downey C. Explorations in Parallel Linear Genetic Programming. [Masters Thesis]. Victoria University of Wellington; 2011. Available from: http://hdl.handle.net/10063/2312

10. Lasek-Nesselquist, Erica. Population biology and Comparative Genomics of Giardia duodenalis Assemblages.

Degree: PhD, Division of Biology and Medicine. Ecological and Evolutionary Biology, 2009, Brown University

 Giardia duodenalis is a major cause of diarrheal disease worldwide and eludes effective characterization at the population level due to the fact that the majority… (more)

Subjects/Keywords: genetic exchange

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APA (6th Edition):

Lasek-Nesselquist, E. (2009). Population biology and Comparative Genomics of Giardia duodenalis Assemblages. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:230/

Chicago Manual of Style (16th Edition):

Lasek-Nesselquist, Erica. “Population biology and Comparative Genomics of Giardia duodenalis Assemblages.” 2009. Doctoral Dissertation, Brown University. Accessed March 28, 2020. https://repository.library.brown.edu/studio/item/bdr:230/.

MLA Handbook (7th Edition):

Lasek-Nesselquist, Erica. “Population biology and Comparative Genomics of Giardia duodenalis Assemblages.” 2009. Web. 28 Mar 2020.

Vancouver:

Lasek-Nesselquist E. Population biology and Comparative Genomics of Giardia duodenalis Assemblages. [Internet] [Doctoral dissertation]. Brown University; 2009. [cited 2020 Mar 28]. Available from: https://repository.library.brown.edu/studio/item/bdr:230/.

Council of Science Editors:

Lasek-Nesselquist E. Population biology and Comparative Genomics of Giardia duodenalis Assemblages. [Doctoral Dissertation]. Brown University; 2009. Available from: https://repository.library.brown.edu/studio/item/bdr:230/


University of Cape Town

11. Al-Kharusi, Khalsa. The experiences of couples undergoing Preimplantation Genetic Diagnosis (PGD) at the Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital (SQUH) in Oman.

Degree: Image, Division of Human Genetics, 2016, University of Cape Town

 Preimplantation genetic diagnosis (PGD) is an alternative reproductive technology integrated with in-vitro fertilisation (IVF). It is a well-established technique offering reproductive options for families at… (more)

Subjects/Keywords: Genetic Counselling

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APA (6th Edition):

Al-Kharusi, K. (2016). The experiences of couples undergoing Preimplantation Genetic Diagnosis (PGD) at the Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital (SQUH) in Oman. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/23776

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):

Al-Kharusi, Khalsa. “The experiences of couples undergoing Preimplantation Genetic Diagnosis (PGD) at the Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital (SQUH) in Oman.” 2016. Thesis, University of Cape Town. Accessed March 28, 2020. http://hdl.handle.net/11427/23776.

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

MLA Handbook (7th Edition):

Al-Kharusi, Khalsa. “The experiences of couples undergoing Preimplantation Genetic Diagnosis (PGD) at the Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital (SQUH) in Oman.” 2016. Web. 28 Mar 2020.

Vancouver:

Al-Kharusi K. The experiences of couples undergoing Preimplantation Genetic Diagnosis (PGD) at the Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital (SQUH) in Oman. [Internet] [Thesis]. University of Cape Town; 2016. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/11427/23776.

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

Council of Science Editors:

Al-Kharusi K. The experiences of couples undergoing Preimplantation Genetic Diagnosis (PGD) at the Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital (SQUH) in Oman. [Thesis]. University of Cape Town; 2016. Available from: http://hdl.handle.net/11427/23776

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


University of Cape Town

12. Ingram, Clair. Perceptions of health-related quality of life among adults living with sickle cell disease in Cape Town, South Africa.

Degree: Image, Division of Human Genetics, 2018, University of Cape Town

 Sickle cell disease (SCD) is a chronic, heritable blood disorder with affected individuals suffering from debilitating health issues and requiring frequent hospitalisation. SCD is highly… (more)

Subjects/Keywords: Genetic Counselling

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APA (6th Edition):

Ingram, C. (2018). Perceptions of health-related quality of life among adults living with sickle cell disease in Cape Town, South Africa. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/27841

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):

Ingram, Clair. “Perceptions of health-related quality of life among adults living with sickle cell disease in Cape Town, South Africa.” 2018. Thesis, University of Cape Town. Accessed March 28, 2020. http://hdl.handle.net/11427/27841.

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

MLA Handbook (7th Edition):

Ingram, Clair. “Perceptions of health-related quality of life among adults living with sickle cell disease in Cape Town, South Africa.” 2018. Web. 28 Mar 2020.

Vancouver:

Ingram C. Perceptions of health-related quality of life among adults living with sickle cell disease in Cape Town, South Africa. [Internet] [Thesis]. University of Cape Town; 2018. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/11427/27841.

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

Council of Science Editors:

Ingram C. Perceptions of health-related quality of life among adults living with sickle cell disease in Cape Town, South Africa. [Thesis]. University of Cape Town; 2018. Available from: http://hdl.handle.net/11427/27841

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


University of Cape Town

13. Verkijk, Nakita. An investigation into the reasons for non-uptake of carrier testing in a family affected by alpha thalassaemia X-linked mental retardation (ATR-X) syndrome.

Degree: Image, Medicine, 2011, University of Cape Town

 Alpha thalassaemia X-linked mental retardation (ATR-X) syndrome is a rare, X-linked intellectual disability syndrome with an estimated prevalence in the range of 1-9/1 000 000.… (more)

Subjects/Keywords: Genetic Counselling

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APA (6th Edition):

Verkijk, N. (2011). An investigation into the reasons for non-uptake of carrier testing in a family affected by alpha thalassaemia X-linked mental retardation (ATR-X) syndrome. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/11481

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):

Verkijk, Nakita. “An investigation into the reasons for non-uptake of carrier testing in a family affected by alpha thalassaemia X-linked mental retardation (ATR-X) syndrome.” 2011. Thesis, University of Cape Town. Accessed March 28, 2020. http://hdl.handle.net/11427/11481.

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

MLA Handbook (7th Edition):

Verkijk, Nakita. “An investigation into the reasons for non-uptake of carrier testing in a family affected by alpha thalassaemia X-linked mental retardation (ATR-X) syndrome.” 2011. Web. 28 Mar 2020.

Vancouver:

Verkijk N. An investigation into the reasons for non-uptake of carrier testing in a family affected by alpha thalassaemia X-linked mental retardation (ATR-X) syndrome. [Internet] [Thesis]. University of Cape Town; 2011. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/11427/11481.

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

Council of Science Editors:

Verkijk N. An investigation into the reasons for non-uptake of carrier testing in a family affected by alpha thalassaemia X-linked mental retardation (ATR-X) syndrome. [Thesis]. University of Cape Town; 2011. Available from: http://hdl.handle.net/11427/11481

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


University of Cape Town

14. Carvill, Gemma. The role of epigenetic factors in the pathogenesis of familial X-linked mental retardation (XLMR).

Degree: Image, Division of Human Genetics, 2010, University of Cape Town

 Mental retardation (MR) is a handicap with severe implications not only for thosethat suffer from this disability, but also for their families, society and the… (more)

Subjects/Keywords: Human Genetic

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APA (6th Edition):

Carvill, G. (2010). The role of epigenetic factors in the pathogenesis of familial X-linked mental retardation (XLMR). (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/3090

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):

Carvill, Gemma. “The role of epigenetic factors in the pathogenesis of familial X-linked mental retardation (XLMR).” 2010. Thesis, University of Cape Town. Accessed March 28, 2020. http://hdl.handle.net/11427/3090.

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

MLA Handbook (7th Edition):

Carvill, Gemma. “The role of epigenetic factors in the pathogenesis of familial X-linked mental retardation (XLMR).” 2010. Web. 28 Mar 2020.

Vancouver:

Carvill G. The role of epigenetic factors in the pathogenesis of familial X-linked mental retardation (XLMR). [Internet] [Thesis]. University of Cape Town; 2010. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/11427/3090.

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

Council of Science Editors:

Carvill G. The role of epigenetic factors in the pathogenesis of familial X-linked mental retardation (XLMR). [Thesis]. University of Cape Town; 2010. Available from: http://hdl.handle.net/11427/3090

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


Wake Forest University

15. Zhou, Xin. Measurements Associated With Learning More Secure Computer Configuration Parameters.

Degree: 2015, Wake Forest University

 To defend against a cyber attack in which the attacker searches the network for vulnerable machines, most people will install some specific security software that… (more)

Subjects/Keywords: Genetic Alogrithm

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

APA (6th Edition):

Zhou, X. (2015). Measurements Associated With Learning More Secure Computer Configuration Parameters. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/57131

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):

Zhou, Xin. “Measurements Associated With Learning More Secure Computer Configuration Parameters.” 2015. Thesis, Wake Forest University. Accessed March 28, 2020. http://hdl.handle.net/10339/57131.

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

MLA Handbook (7th Edition):

Zhou, Xin. “Measurements Associated With Learning More Secure Computer Configuration Parameters.” 2015. Web. 28 Mar 2020.

Vancouver:

Zhou X. Measurements Associated With Learning More Secure Computer Configuration Parameters. [Internet] [Thesis]. Wake Forest University; 2015. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10339/57131.

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

Council of Science Editors:

Zhou X. Measurements Associated With Learning More Secure Computer Configuration Parameters. [Thesis]. Wake Forest University; 2015. Available from: http://hdl.handle.net/10339/57131

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


Harvard University

16. O'Connor, Luke Jen. Genetic Architecture of Common Diseases and Complex Traits.

Degree: PhD, 2019, Harvard University

Over the last decade, genome-wide association studies (GWAS) have revolutionized the study of disease. For the first time, the genetic architectures of common diseases and… (more)

Subjects/Keywords: Genetic architecture

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

APA (6th Edition):

O'Connor, L. J. (2019). Genetic Architecture of Common Diseases and Complex Traits. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029501

Chicago Manual of Style (16th Edition):

O'Connor, Luke Jen. “Genetic Architecture of Common Diseases and Complex Traits.” 2019. Doctoral Dissertation, Harvard University. Accessed March 28, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029501.

MLA Handbook (7th Edition):

O'Connor, Luke Jen. “Genetic Architecture of Common Diseases and Complex Traits.” 2019. Web. 28 Mar 2020.

Vancouver:

O'Connor LJ. Genetic Architecture of Common Diseases and Complex Traits. [Internet] [Doctoral dissertation]. Harvard University; 2019. [cited 2020 Mar 28]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029501.

Council of Science Editors:

O'Connor LJ. Genetic Architecture of Common Diseases and Complex Traits. [Doctoral Dissertation]. Harvard University; 2019. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029501


University of Cape Town

17. Malope, Malebo Felicia. Exploring the decision making process of women offered termination of pregnancy for serious congenital abnormality.

Degree: Image, Division of Human Genetics, 2018, University of Cape Town

 Background: A weekly pregnancy counselling clinic is held in conjunction with foetal medicine experts at Groote Schuur Hospital for women with pregnancies complicated by foetal… (more)

Subjects/Keywords: Genetic Counselling

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

APA (6th Edition):

Malope, . M. F. (2018). Exploring the decision making process of women offered termination of pregnancy for serious congenital abnormality. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/27900

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):

Malope, Malebo Felicia. “Exploring the decision making process of women offered termination of pregnancy for serious congenital abnormality.” 2018. Thesis, University of Cape Town. Accessed March 28, 2020. http://hdl.handle.net/11427/27900.

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

MLA Handbook (7th Edition):

Malope, Malebo Felicia. “Exploring the decision making process of women offered termination of pregnancy for serious congenital abnormality.” 2018. Web. 28 Mar 2020.

Vancouver:

Malope MF. Exploring the decision making process of women offered termination of pregnancy for serious congenital abnormality. [Internet] [Thesis]. University of Cape Town; 2018. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/11427/27900.

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

Council of Science Editors:

Malope MF. Exploring the decision making process of women offered termination of pregnancy for serious congenital abnormality. [Thesis]. University of Cape Town; 2018. Available from: http://hdl.handle.net/11427/27900

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

18. Guay, Catherine L., 1979-. High-throughput tools for functional genomics.

Degree: PhD, Computational and Integrative Biology, 2018, Rutgers University

Genetic information is stored in DNA sequences, referred to as the genome. Decoding the meaning of these sequences is a critical challenge in biology. The… (more)

Subjects/Keywords: Genetic regulation

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

APA (6th Edition):

Guay, Catherine L., 1. (2018). High-throughput tools for functional genomics. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/57076/

Chicago Manual of Style (16th Edition):

Guay, Catherine L., 1979-. “High-throughput tools for functional genomics.” 2018. Doctoral Dissertation, Rutgers University. Accessed March 28, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/57076/.

MLA Handbook (7th Edition):

Guay, Catherine L., 1979-. “High-throughput tools for functional genomics.” 2018. Web. 28 Mar 2020.

Vancouver:

Guay, Catherine L. 1. High-throughput tools for functional genomics. [Internet] [Doctoral dissertation]. Rutgers University; 2018. [cited 2020 Mar 28]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/57076/.

Council of Science Editors:

Guay, Catherine L. 1. High-throughput tools for functional genomics. [Doctoral Dissertation]. Rutgers University; 2018. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/57076/


George Mason University

19. Wilbert, Tammy R. Patterns and Processes of Genetic Diversity in the Endangered San Joaquin Kit Fox .

Degree: 2014, George Mason University

 Survival of the endangered San Joaquin kit fox (SJKF; Vulpes macrotis mutica) is challenged by reduced and fragmented habitat resulting from anthropogenic land uses in… (more)

Subjects/Keywords: genetic diversity

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APA (6th Edition):

Wilbert, T. R. (2014). Patterns and Processes of Genetic Diversity in the Endangered San Joaquin Kit Fox . (Thesis). George Mason University. Retrieved from http://hdl.handle.net/1920/8936

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):

Wilbert, Tammy R. “Patterns and Processes of Genetic Diversity in the Endangered San Joaquin Kit Fox .” 2014. Thesis, George Mason University. Accessed March 28, 2020. http://hdl.handle.net/1920/8936.

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

MLA Handbook (7th Edition):

Wilbert, Tammy R. “Patterns and Processes of Genetic Diversity in the Endangered San Joaquin Kit Fox .” 2014. Web. 28 Mar 2020.

Vancouver:

Wilbert TR. Patterns and Processes of Genetic Diversity in the Endangered San Joaquin Kit Fox . [Internet] [Thesis]. George Mason University; 2014. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/1920/8936.

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

Council of Science Editors:

Wilbert TR. Patterns and Processes of Genetic Diversity in the Endangered San Joaquin Kit Fox . [Thesis]. George Mason University; 2014. Available from: http://hdl.handle.net/1920/8936

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


University of Cape Town

20. Shaw, Tarryn. Women's experiences of receiving a child's fetal alcohol spectrum disorder diagnosis: a Western Cape study.

Degree: Image, Division of Human Genetics, 2015, University of Cape Town

 There are a range of conditions, collectively known as fetal alcohol spectrum disorders (FASD), which result from the exposure of a developing fetus to alcohol.… (more)

Subjects/Keywords: Genetic Counselling

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

APA (6th Edition):

Shaw, T. (2015). Women's experiences of receiving a child's fetal alcohol spectrum disorder diagnosis: a Western Cape study. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/16922

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):

Shaw, Tarryn. “Women's experiences of receiving a child's fetal alcohol spectrum disorder diagnosis: a Western Cape study.” 2015. Thesis, University of Cape Town. Accessed March 28, 2020. http://hdl.handle.net/11427/16922.

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

MLA Handbook (7th Edition):

Shaw, Tarryn. “Women's experiences of receiving a child's fetal alcohol spectrum disorder diagnosis: a Western Cape study.” 2015. Web. 28 Mar 2020.

Vancouver:

Shaw T. Women's experiences of receiving a child's fetal alcohol spectrum disorder diagnosis: a Western Cape study. [Internet] [Thesis]. University of Cape Town; 2015. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/11427/16922.

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

Council of Science Editors:

Shaw T. Women's experiences of receiving a child's fetal alcohol spectrum disorder diagnosis: a Western Cape study. [Thesis]. University of Cape Town; 2015. Available from: http://hdl.handle.net/11427/16922

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


University of Cape Town

21. du Toit, Maxine. The role of a genetic counsellor in a support group for Huntington disease.

Degree: MSc, Clinical Laboratory Sciences, 2019, University of Cape Town

Genetic counselling students are encouraged to become involved with support groups for genetic conditions. However, their roles within these groups are not well defined and… (more)

Subjects/Keywords: Genetic Counselling

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

APA (6th Edition):

du Toit, M. (2019). The role of a genetic counsellor in a support group for Huntington disease. (Masters Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/31543

Chicago Manual of Style (16th Edition):

du Toit, Maxine. “The role of a genetic counsellor in a support group for Huntington disease.” 2019. Masters Thesis, University of Cape Town. Accessed March 28, 2020. http://hdl.handle.net/11427/31543.

MLA Handbook (7th Edition):

du Toit, Maxine. “The role of a genetic counsellor in a support group for Huntington disease.” 2019. Web. 28 Mar 2020.

Vancouver:

du Toit M. The role of a genetic counsellor in a support group for Huntington disease. [Internet] [Masters thesis]. University of Cape Town; 2019. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/11427/31543.

Council of Science Editors:

du Toit M. The role of a genetic counsellor in a support group for Huntington disease. [Masters Thesis]. University of Cape Town; 2019. Available from: http://hdl.handle.net/11427/31543


Brandeis University

22. Liberman, Stacey. To Be a Clinical or Non-Clinical Genetic Counselor, That is the Question.

Degree: 2016, Brandeis University

 Many genetic counselors are leaving or considering leaving their clinical positions for non-clinical positions. This comes at a time when there is an increasing need… (more)

Subjects/Keywords: genetic counseling roles; clinical genetic counselors; non-clinical genetic counselors; genetic counseling students; genetic counseling workforce; industry; genetic counselor demand

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

APA (6th Edition):

Liberman, S. (2016). To Be a Clinical or Non-Clinical Genetic Counselor, That is the Question. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/32087

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):

Liberman, Stacey. “To Be a Clinical or Non-Clinical Genetic Counselor, That is the Question.” 2016. Thesis, Brandeis University. Accessed March 28, 2020. http://hdl.handle.net/10192/32087.

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

MLA Handbook (7th Edition):

Liberman, Stacey. “To Be a Clinical or Non-Clinical Genetic Counselor, That is the Question.” 2016. Web. 28 Mar 2020.

Vancouver:

Liberman S. To Be a Clinical or Non-Clinical Genetic Counselor, That is the Question. [Internet] [Thesis]. Brandeis University; 2016. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10192/32087.

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

Council of Science Editors:

Liberman S. To Be a Clinical or Non-Clinical Genetic Counselor, That is the Question. [Thesis]. Brandeis University; 2016. Available from: http://hdl.handle.net/10192/32087

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


Laurentian University

23. Laurence, Sophie. Genetic variation and population genetic structure of muskrat, Ondatra Zibethicus, at different spatial scales .

Degree: 2014, Laurentian University

 Understanding the factors and processes that influence intraspecific genetic variation are essential to better understand evolutionary processes. In this research, I examined patterns of gene… (more)

Subjects/Keywords: Genetic variation; Population genetic structure; Muskrat

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APA (6th Edition):

Laurence, S. (2014). Genetic variation and population genetic structure of muskrat, Ondatra Zibethicus, at different spatial scales . (Thesis). Laurentian University. Retrieved from https://zone.biblio.laurentian.ca/dspace/handle/10219/2171

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):

Laurence, Sophie. “Genetic variation and population genetic structure of muskrat, Ondatra Zibethicus, at different spatial scales .” 2014. Thesis, Laurentian University. Accessed March 28, 2020. https://zone.biblio.laurentian.ca/dspace/handle/10219/2171.

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

MLA Handbook (7th Edition):

Laurence, Sophie. “Genetic variation and population genetic structure of muskrat, Ondatra Zibethicus, at different spatial scales .” 2014. Web. 28 Mar 2020.

Vancouver:

Laurence S. Genetic variation and population genetic structure of muskrat, Ondatra Zibethicus, at different spatial scales . [Internet] [Thesis]. Laurentian University; 2014. [cited 2020 Mar 28]. Available from: https://zone.biblio.laurentian.ca/dspace/handle/10219/2171.

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

Council of Science Editors:

Laurence S. Genetic variation and population genetic structure of muskrat, Ondatra Zibethicus, at different spatial scales . [Thesis]. Laurentian University; 2014. Available from: https://zone.biblio.laurentian.ca/dspace/handle/10219/2171

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


University of Hong Kong

24. 蘇寶琳; So, Po-lam. Overview of parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong and implication for genetic counselling.

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

 Objectives With advancement of technology in genetic testing and widespread use of prenatal diagnosis, the prenatal detection of sex chromosome aneuploidies (SCA) is often unavoidable.… (more)

Subjects/Keywords: Genetic disorders; Prenatal diagnosis; Genetic counseling

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

APA (6th Edition):

蘇寶琳; So, P. (2015). Overview of parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong and implication for genetic counselling. (Masters Thesis). University of Hong Kong. Retrieved from So, P. [蘇寶琳]. (2015). Overview of parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong and implication for genetic counselling. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5734121 ; http://hdl.handle.net/10722/225095

Chicago Manual of Style (16th Edition):

蘇寶琳; So, Po-lam. “Overview of parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong and implication for genetic counselling.” 2015. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. So, P. [蘇寶琳]. (2015). Overview of parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong and implication for genetic counselling. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5734121 ; http://hdl.handle.net/10722/225095.

MLA Handbook (7th Edition):

蘇寶琳; So, Po-lam. “Overview of parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong and implication for genetic counselling.” 2015. Web. 28 Mar 2020.

Vancouver:

蘇寶琳; So P. Overview of parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong and implication for genetic counselling. [Internet] [Masters thesis]. University of Hong Kong; 2015. [cited 2020 Mar 28]. Available from: So, P. [蘇寶琳]. (2015). Overview of parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong and implication for genetic counselling. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5734121 ; http://hdl.handle.net/10722/225095.

Council of Science Editors:

蘇寶琳; So P. Overview of parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong and implication for genetic counselling. [Masters Thesis]. University of Hong Kong; 2015. Available from: So, P. [蘇寶琳]. (2015). Overview of parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong and implication for genetic counselling. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5734121 ; http://hdl.handle.net/10722/225095


University of Hong Kong

25. 鄭靜恩; Cheng, Ching-yan, Serene. Impact of Non-invasive Prenatal Testing on genetic counselling, invasive prenatal diagnosis and atypical chromosomal anomalies detection.

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

Aneuploidy is one of the known major causes of miscarriage and congenital birth defects. It refers to chromosomal abnormality with chromosome number being different from… (more)

Subjects/Keywords: Genetic counseling; Prenatal diagnosis; Genetic disorders

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APA (6th Edition):

鄭靜恩; Cheng, Ching-yan, S. (2017). Impact of Non-invasive Prenatal Testing on genetic counselling, invasive prenatal diagnosis and atypical chromosomal anomalies detection. (Masters Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/251327

Chicago Manual of Style (16th Edition):

鄭靜恩; Cheng, Ching-yan, Serene. “Impact of Non-invasive Prenatal Testing on genetic counselling, invasive prenatal diagnosis and atypical chromosomal anomalies detection.” 2017. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. http://hdl.handle.net/10722/251327.

MLA Handbook (7th Edition):

鄭靜恩; Cheng, Ching-yan, Serene. “Impact of Non-invasive Prenatal Testing on genetic counselling, invasive prenatal diagnosis and atypical chromosomal anomalies detection.” 2017. Web. 28 Mar 2020.

Vancouver:

鄭靜恩; Cheng, Ching-yan S. Impact of Non-invasive Prenatal Testing on genetic counselling, invasive prenatal diagnosis and atypical chromosomal anomalies detection. [Internet] [Masters thesis]. University of Hong Kong; 2017. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10722/251327.

Council of Science Editors:

鄭靜恩; Cheng, Ching-yan S. Impact of Non-invasive Prenatal Testing on genetic counselling, invasive prenatal diagnosis and atypical chromosomal anomalies detection. [Masters Thesis]. University of Hong Kong; 2017. Available from: http://hdl.handle.net/10722/251327


University of Hong Kong

26. Ng, Pik-ying, Paulina. Prenatally diagnosed small supernumerary marker chromosomes in Hong Kong : the science and the challenge in genetic counselling.

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

 Background and Objectives: Small supernumerary marker chromosomes are abnormal findings in prenatal cytogenetic testing and prognosis of an individual carrying a marker chromosome varies with… (more)

Subjects/Keywords: Genetic disorders - China - Hong Kong; Genetic counseling

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APA (6th Edition):

Ng, Pik-ying, P. (2015). Prenatally diagnosed small supernumerary marker chromosomes in Hong Kong : the science and the challenge in genetic counselling. (Masters Thesis). University of Hong Kong. Retrieved from Ng, P. P. [吳碧英]. (2015). Prenatally diagnosed small supernumerary marker chromosomes in Hong Kong : the science and the challenge in genetic counselling. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5659406 ; http://hdl.handle.net/10722/221483

Chicago Manual of Style (16th Edition):

Ng, Pik-ying, Paulina. “Prenatally diagnosed small supernumerary marker chromosomes in Hong Kong : the science and the challenge in genetic counselling.” 2015. Masters Thesis, University of Hong Kong. Accessed March 28, 2020. Ng, P. P. [吳碧英]. (2015). Prenatally diagnosed small supernumerary marker chromosomes in Hong Kong : the science and the challenge in genetic counselling. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5659406 ; http://hdl.handle.net/10722/221483.

MLA Handbook (7th Edition):

Ng, Pik-ying, Paulina. “Prenatally diagnosed small supernumerary marker chromosomes in Hong Kong : the science and the challenge in genetic counselling.” 2015. Web. 28 Mar 2020.

Vancouver:

Ng, Pik-ying P. Prenatally diagnosed small supernumerary marker chromosomes in Hong Kong : the science and the challenge in genetic counselling. [Internet] [Masters thesis]. University of Hong Kong; 2015. [cited 2020 Mar 28]. Available from: Ng, P. P. [吳碧英]. (2015). Prenatally diagnosed small supernumerary marker chromosomes in Hong Kong : the science and the challenge in genetic counselling. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5659406 ; http://hdl.handle.net/10722/221483.

Council of Science Editors:

Ng, Pik-ying P. Prenatally diagnosed small supernumerary marker chromosomes in Hong Kong : the science and the challenge in genetic counselling. [Masters Thesis]. University of Hong Kong; 2015. Available from: Ng, P. P. [吳碧英]. (2015). Prenatally diagnosed small supernumerary marker chromosomes in Hong Kong : the science and the challenge in genetic counselling. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5659406 ; http://hdl.handle.net/10722/221483


University of Hong Kong

27. 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 March 28, 2020. 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. 28 Mar 2020.

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 2020 Mar 28]. 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 Hong Kong

28. 郭友玲; Guo, Youling. Genetic and genomic mapping of common diseases.

Degree: PhD, 2012, University of Hong Kong

 Genome-wide mapping of susceptibility genes was conducted in two complex disorders of hypertension and epilepsy, allowing the dissection of the genetic architecture of these… (more)

Subjects/Keywords: Epilepsy - Genetic aspects.; Hypertension - Genetic aspects.

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

APA (6th Edition):

郭友玲; Guo, Y. (2012). Genetic and genomic mapping of common diseases. (Doctoral Dissertation). University of Hong Kong. Retrieved from Guo, Y. [郭友玲]. (2012). Genetic and genomic mapping of common diseases. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5053386 ; http://dx.doi.org/10.5353/th_b5053386 ; http://hdl.handle.net/10722/188267

Chicago Manual of Style (16th Edition):

郭友玲; Guo, Youling. “Genetic and genomic mapping of common diseases.” 2012. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Guo, Y. [郭友玲]. (2012). Genetic and genomic mapping of common diseases. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5053386 ; http://dx.doi.org/10.5353/th_b5053386 ; http://hdl.handle.net/10722/188267.

MLA Handbook (7th Edition):

郭友玲; Guo, Youling. “Genetic and genomic mapping of common diseases.” 2012. Web. 28 Mar 2020.

Vancouver:

郭友玲; Guo Y. Genetic and genomic mapping of common diseases. [Internet] [Doctoral dissertation]. University of Hong Kong; 2012. [cited 2020 Mar 28]. Available from: Guo, Y. [郭友玲]. (2012). Genetic and genomic mapping of common diseases. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5053386 ; http://dx.doi.org/10.5353/th_b5053386 ; http://hdl.handle.net/10722/188267.

Council of Science Editors:

郭友玲; Guo Y. Genetic and genomic mapping of common diseases. [Doctoral Dissertation]. University of Hong Kong; 2012. Available from: Guo, Y. [郭友玲]. (2012). Genetic and genomic mapping of common diseases. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5053386 ; http://dx.doi.org/10.5353/th_b5053386 ; http://hdl.handle.net/10722/188267


University of Hong Kong

29. Wong, Hoi-man, Emily. Genome-wide association analyses on complex diseases: from single-nucleotide polymorphism to copy numbervariation.

Degree: PhD, 2013, University of Hong Kong

 Complex diseases, unlike Mendialian diseases, are often characterized by genetic heterogeneity and multifactorial inheritance, involving defects in genes from the same or multiple alternative pathways.… (more)

Subjects/Keywords: Abnormalities, Human - Genetic aspects.; Schizophrenia - Genetic aspects.

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APA (6th Edition):

Wong, Hoi-man, E. (2013). Genome-wide association analyses on complex diseases: from single-nucleotide polymorphism to copy numbervariation. (Doctoral Dissertation). University of Hong Kong. Retrieved from Wong, H. E. [黃凱敏]. (2013). Genome-wide association analyses on complex diseases : from single-nucleotide polymorphism to copy number variation. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5053409 ; http://dx.doi.org/10.5353/th_b5053409 ; http://hdl.handle.net/10722/188290

Chicago Manual of Style (16th Edition):

Wong, Hoi-man, Emily. “Genome-wide association analyses on complex diseases: from single-nucleotide polymorphism to copy numbervariation.” 2013. Doctoral Dissertation, University of Hong Kong. Accessed March 28, 2020. Wong, H. E. [黃凱敏]. (2013). Genome-wide association analyses on complex diseases : from single-nucleotide polymorphism to copy number variation. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5053409 ; http://dx.doi.org/10.5353/th_b5053409 ; http://hdl.handle.net/10722/188290.

MLA Handbook (7th Edition):

Wong, Hoi-man, Emily. “Genome-wide association analyses on complex diseases: from single-nucleotide polymorphism to copy numbervariation.” 2013. Web. 28 Mar 2020.

Vancouver:

Wong, Hoi-man E. Genome-wide association analyses on complex diseases: from single-nucleotide polymorphism to copy numbervariation. [Internet] [Doctoral dissertation]. University of Hong Kong; 2013. [cited 2020 Mar 28]. Available from: Wong, H. E. [黃凱敏]. (2013). Genome-wide association analyses on complex diseases : from single-nucleotide polymorphism to copy number variation. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5053409 ; http://dx.doi.org/10.5353/th_b5053409 ; http://hdl.handle.net/10722/188290.

Council of Science Editors:

Wong, Hoi-man E. Genome-wide association analyses on complex diseases: from single-nucleotide polymorphism to copy numbervariation. [Doctoral Dissertation]. University of Hong Kong; 2013. Available from: Wong, H. E. [黃凱敏]. (2013). Genome-wide association analyses on complex diseases : from single-nucleotide polymorphism to copy number variation. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5053409 ; http://dx.doi.org/10.5353/th_b5053409 ; http://hdl.handle.net/10722/188290


NSYSU

30. Chung, Chia-ying. Genetic diversity, genetic divergence and phylogeographical patterns in Calocedrus based on microsatellites.

Degree: Master, Biological Sciences, 2015, NSYSU

 The genus Calocedrus is Eastern Asian â North American disjunctive distribution. Calocedrus formosana (Florin) Florin is restricted to Taiwan, Calocedrus macrolepis Kurz, and C. rupestris… (more)

Subjects/Keywords: genetic diversity; genetic differentiation; microsatellite; phylogeographical; Calocedrus

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APA (6th Edition):

Chung, C. (2015). Genetic diversity, genetic divergence and phylogeographical patterns in Calocedrus based on microsatellites. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0724115-101740

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):

Chung, Chia-ying. “Genetic diversity, genetic divergence and phylogeographical patterns in Calocedrus based on microsatellites.” 2015. Thesis, NSYSU. Accessed March 28, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0724115-101740.

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

MLA Handbook (7th Edition):

Chung, Chia-ying. “Genetic diversity, genetic divergence and phylogeographical patterns in Calocedrus based on microsatellites.” 2015. Web. 28 Mar 2020.

Vancouver:

Chung C. Genetic diversity, genetic divergence and phylogeographical patterns in Calocedrus based on microsatellites. [Internet] [Thesis]. NSYSU; 2015. [cited 2020 Mar 28]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0724115-101740.

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

Council of Science Editors:

Chung C. Genetic diversity, genetic divergence and phylogeographical patterns in Calocedrus based on microsatellites. [Thesis]. NSYSU; 2015. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0724115-101740

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

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