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You searched for subject:(human genetics). Showing records 1 – 30 of 726 total matches.

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University of Cape Town

1. Dalvie, Shareefa. Genetic analysis of bipolar disorder and alcohol use disorder.

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

 Background: Mental health disorders represent a major public health problem in most countries around the world. In South Africa, the lifetime prevalence of psychiatric disorders… (more)

Subjects/Keywords: Human Genetics

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

APA (6th Edition):

Dalvie, S. (2015). Genetic analysis of bipolar disorder and alcohol use disorder. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/16560

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):

Dalvie, Shareefa. “Genetic analysis of bipolar disorder and alcohol use disorder.” 2015. Thesis, University of Cape Town. Accessed April 17, 2021. http://hdl.handle.net/11427/16560.

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

MLA Handbook (7th Edition):

Dalvie, Shareefa. “Genetic analysis of bipolar disorder and alcohol use disorder.” 2015. Web. 17 Apr 2021.

Vancouver:

Dalvie S. Genetic analysis of bipolar disorder and alcohol use disorder. [Internet] [Thesis]. University of Cape Town; 2015. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11427/16560.

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

Council of Science Editors:

Dalvie S. Genetic analysis of bipolar disorder and alcohol use disorder. [Thesis]. University of Cape Town; 2015. Available from: http://hdl.handle.net/11427/16560

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


University of Cape Town

2. Watson, Lauren. Novel cell models for the study of spinocerebellar ataxia type 7 pathogenesis and therapy in a South African patient cohort.

Degree: Image, Division of Human Genetics, 2012, University of Cape Town

 Spinocerebellar ataxia type 7 (SCA7) is a dominantly-inherited neurodegenerative disease, resulting from a CAG trinucleotide repeat expansion in the ataxin-7 gene. The Ataxin-7 protein is… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Watson, L. (2012). Novel cell models for the study of spinocerebellar ataxia type 7 pathogenesis and therapy in a South African patient cohort. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/3108

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):

Watson, Lauren. “Novel cell models for the study of spinocerebellar ataxia type 7 pathogenesis and therapy in a South African patient cohort.” 2012. Thesis, University of Cape Town. Accessed April 17, 2021. http://hdl.handle.net/11427/3108.

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

MLA Handbook (7th Edition):

Watson, Lauren. “Novel cell models for the study of spinocerebellar ataxia type 7 pathogenesis and therapy in a South African patient cohort.” 2012. Web. 17 Apr 2021.

Vancouver:

Watson L. Novel cell models for the study of spinocerebellar ataxia type 7 pathogenesis and therapy in a South African patient cohort. [Internet] [Thesis]. University of Cape Town; 2012. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11427/3108.

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

Council of Science Editors:

Watson L. Novel cell models for the study of spinocerebellar ataxia type 7 pathogenesis and therapy in a South African patient cohort. [Thesis]. University of Cape Town; 2012. Available from: http://hdl.handle.net/11427/3108

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


University of Cape Town

3. Pule, Gift Dineo. Study of genetic modifiers of fetal hemoglobin and mechanisms of hydroxyurea-induced γ-globin expression in sickle cell disease.

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

 Sickle Cell Disease (SCD) is a growing global problem with firm roots in sub-Saharan Africa (SSA) representing over 3/4 of the global burden of the… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Pule, G. D. (2016). Study of genetic modifiers of fetal hemoglobin and mechanisms of hydroxyurea-induced γ-globin expression in sickle cell disease. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/22730

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):

Pule, Gift Dineo. “Study of genetic modifiers of fetal hemoglobin and mechanisms of hydroxyurea-induced γ-globin expression in sickle cell disease.” 2016. Thesis, University of Cape Town. Accessed April 17, 2021. http://hdl.handle.net/11427/22730.

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

MLA Handbook (7th Edition):

Pule, Gift Dineo. “Study of genetic modifiers of fetal hemoglobin and mechanisms of hydroxyurea-induced γ-globin expression in sickle cell disease.” 2016. Web. 17 Apr 2021.

Vancouver:

Pule GD. Study of genetic modifiers of fetal hemoglobin and mechanisms of hydroxyurea-induced γ-globin expression in sickle cell disease. [Internet] [Thesis]. University of Cape Town; 2016. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11427/22730.

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

Council of Science Editors:

Pule GD. Study of genetic modifiers of fetal hemoglobin and mechanisms of hydroxyurea-induced γ-globin expression in sickle cell disease. [Thesis]. University of Cape Town; 2016. Available from: http://hdl.handle.net/11427/22730

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


University of Cape Town

4. Roberts, Lisa Jane. Genetic analysis of inherited retinal diseases in indigenous Southern African populations.

Degree: Image, Division of Human Genetics, 2017, University of Cape Town

 Background: Inherited retinal diseases (IRDs) constitute a group of clinically and genetically heterogeneous conditions which cause degeneration of retinal photoreceptor cells and result in visual… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Roberts, L. J. (2017). Genetic analysis of inherited retinal diseases in indigenous Southern African populations. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/25419

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):

Roberts, Lisa Jane. “Genetic analysis of inherited retinal diseases in indigenous Southern African populations.” 2017. Thesis, University of Cape Town. Accessed April 17, 2021. http://hdl.handle.net/11427/25419.

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

MLA Handbook (7th Edition):

Roberts, Lisa Jane. “Genetic analysis of inherited retinal diseases in indigenous Southern African populations.” 2017. Web. 17 Apr 2021.

Vancouver:

Roberts LJ. Genetic analysis of inherited retinal diseases in indigenous Southern African populations. [Internet] [Thesis]. University of Cape Town; 2017. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11427/25419.

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

Council of Science Editors:

Roberts LJ. Genetic analysis of inherited retinal diseases in indigenous Southern African populations. [Thesis]. University of Cape Town; 2017. Available from: http://hdl.handle.net/11427/25419

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


University of Cape Town

5. Lamola, Lindiwe. Genomics of Lynch syndrome and Constitutional mismatch repair deficiency syndrome.

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

 Introduction: The mismatch repair system plays an important role in maintaining the genome integrity as it functions to correct mismatches during DNA replication. Heterozygous mutations… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Lamola, L. (2018). Genomics of Lynch syndrome and Constitutional mismatch repair deficiency syndrome. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/27840

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):

Lamola, Lindiwe. “Genomics of Lynch syndrome and Constitutional mismatch repair deficiency syndrome.” 2018. Thesis, University of Cape Town. Accessed April 17, 2021. http://hdl.handle.net/11427/27840.

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

MLA Handbook (7th Edition):

Lamola, Lindiwe. “Genomics of Lynch syndrome and Constitutional mismatch repair deficiency syndrome.” 2018. Web. 17 Apr 2021.

Vancouver:

Lamola L. Genomics of Lynch syndrome and Constitutional mismatch repair deficiency syndrome. [Internet] [Thesis]. University of Cape Town; 2018. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11427/27840.

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

Council of Science Editors:

Lamola L. Genomics of Lynch syndrome and Constitutional mismatch repair deficiency syndrome. [Thesis]. University of Cape Town; 2018. Available from: http://hdl.handle.net/11427/27840

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


University of Cape Town

6. Smith, Danielle Claire. Spinocerebellar ataxia type 7 in southern africa: an epidemiological, molecular and cellular study.

Degree: Image, Clinical Laboratory Sciences, 2014, University of Cape Town

 Spinocerebellar ataxia type 7 (SCA7) is an inherited neurodegenerative disease caused by a pathogenic expansion of a CAG repeat within the ataxin 7 gene, resulting… (more)

Subjects/Keywords: Human Genetics

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

APA (6th Edition):

Smith, D. C. (2014). Spinocerebellar ataxia type 7 in southern africa: an epidemiological, molecular and cellular study. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/13022

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):

Smith, Danielle Claire. “Spinocerebellar ataxia type 7 in southern africa: an epidemiological, molecular and cellular study.” 2014. Thesis, University of Cape Town. Accessed April 17, 2021. http://hdl.handle.net/11427/13022.

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

MLA Handbook (7th Edition):

Smith, Danielle Claire. “Spinocerebellar ataxia type 7 in southern africa: an epidemiological, molecular and cellular study.” 2014. Web. 17 Apr 2021.

Vancouver:

Smith DC. Spinocerebellar ataxia type 7 in southern africa: an epidemiological, molecular and cellular study. [Internet] [Thesis]. University of Cape Town; 2014. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11427/13022.

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

Council of Science Editors:

Smith DC. Spinocerebellar ataxia type 7 in southern africa: an epidemiological, molecular and cellular study. [Thesis]. University of Cape Town; 2014. Available from: http://hdl.handle.net/11427/13022

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


Universidad de Cantabria

7. Vázquez Bourgon, Javier. DISC1 y psicosis no afectiva : variaciones en endofenotipos y características clínicas en primeros episodios de psicosis: DISC1 and non-affective psychosis : effect on endophenotypes and clinical characteristics in first episode psychosis.

Degree: 2016, Universidad de Cantabria

 RESUMEN: Antecedentes La esquizofrenia es un trastorno psiquiátrico grave, resultante de la interacción conjunta de múltiples factores ambientales y genéticos. El gen Disrupted-in-Schizophrenia 1 (DISC1)… (more)

Subjects/Keywords: Human genetics

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APA (6th Edition):

Vázquez Bourgon, J. (2016). DISC1 y psicosis no afectiva : variaciones en endofenotipos y características clínicas en primeros episodios de psicosis: DISC1 and non-affective psychosis : effect on endophenotypes and clinical characteristics in first episode psychosis. (Doctoral Dissertation). Universidad de Cantabria. Retrieved from http://hdl.handle.net/10902/11940

Chicago Manual of Style (16th Edition):

Vázquez Bourgon, Javier. “DISC1 y psicosis no afectiva : variaciones en endofenotipos y características clínicas en primeros episodios de psicosis: DISC1 and non-affective psychosis : effect on endophenotypes and clinical characteristics in first episode psychosis.” 2016. Doctoral Dissertation, Universidad de Cantabria. Accessed April 17, 2021. http://hdl.handle.net/10902/11940.

MLA Handbook (7th Edition):

Vázquez Bourgon, Javier. “DISC1 y psicosis no afectiva : variaciones en endofenotipos y características clínicas en primeros episodios de psicosis: DISC1 and non-affective psychosis : effect on endophenotypes and clinical characteristics in first episode psychosis.” 2016. Web. 17 Apr 2021.

Vancouver:

Vázquez Bourgon J. DISC1 y psicosis no afectiva : variaciones en endofenotipos y características clínicas en primeros episodios de psicosis: DISC1 and non-affective psychosis : effect on endophenotypes and clinical characteristics in first episode psychosis. [Internet] [Doctoral dissertation]. Universidad de Cantabria; 2016. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/10902/11940.

Council of Science Editors:

Vázquez Bourgon J. DISC1 y psicosis no afectiva : variaciones en endofenotipos y características clínicas en primeros episodios de psicosis: DISC1 and non-affective psychosis : effect on endophenotypes and clinical characteristics in first episode psychosis. [Doctoral Dissertation]. Universidad de Cantabria; 2016. Available from: http://hdl.handle.net/10902/11940


University of Cape Town

8. Baard, Johannes. Genetics of age-related macular degeneration and Stargardt disease in South African populations.

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

 Background: The Retinal Degenerative Diseases (RDD) Research Group in the Division of Human Genetics at UCT has for the past 25 years been intensively investigating… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Baard, J. (2016). Genetics of age-related macular degeneration and Stargardt disease in South African populations. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/20328

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):

Baard, Johannes. “Genetics of age-related macular degeneration and Stargardt disease in South African populations.” 2016. Thesis, University of Cape Town. Accessed April 17, 2021. http://hdl.handle.net/11427/20328.

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

MLA Handbook (7th Edition):

Baard, Johannes. “Genetics of age-related macular degeneration and Stargardt disease in South African populations.” 2016. Web. 17 Apr 2021.

Vancouver:

Baard J. Genetics of age-related macular degeneration and Stargardt disease in South African populations. [Internet] [Thesis]. University of Cape Town; 2016. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11427/20328.

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

Council of Science Editors:

Baard J. Genetics of age-related macular degeneration and Stargardt disease in South African populations. [Thesis]. University of Cape Town; 2016. Available from: http://hdl.handle.net/11427/20328

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


University of Cape Town

9. Mpeta, Bafokeng. The pharmacologenetics of lopinavir in a cohort of black African HIV/AIDS patients.

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

 The Sub-Saharan African region remains the most severely affected by the HIV/AIDS epidemic. At the end of 2011, The Joint United Nations Programme on HIV/AIDS… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Mpeta, B. (2015). The pharmacologenetics of lopinavir in a cohort of black African HIV/AIDS patients. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/15598

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):

Mpeta, Bafokeng. “The pharmacologenetics of lopinavir in a cohort of black African HIV/AIDS patients.” 2015. Thesis, University of Cape Town. Accessed April 17, 2021. http://hdl.handle.net/11427/15598.

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

MLA Handbook (7th Edition):

Mpeta, Bafokeng. “The pharmacologenetics of lopinavir in a cohort of black African HIV/AIDS patients.” 2015. Web. 17 Apr 2021.

Vancouver:

Mpeta B. The pharmacologenetics of lopinavir in a cohort of black African HIV/AIDS patients. [Internet] [Thesis]. University of Cape Town; 2015. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11427/15598.

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

Council of Science Editors:

Mpeta B. The pharmacologenetics of lopinavir in a cohort of black African HIV/AIDS patients. [Thesis]. University of Cape Town; 2015. Available from: http://hdl.handle.net/11427/15598

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


University of Cape Town

10. Bruwer, Zandré. An investigation into factors which have an impact on access to and utilisation of the genetic and endoscopic surveillance clinic offered to high-risk members of known Lynch families.

Degree: Image, Division of Human Genetics, 2011, University of Cape Town

 The Genetic and Endoscopic Surveillance Clinic provides predictive testing and life-saving colorectal cancer screening services to individuals with Lynch syndrome in the Western and Northern… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Bruwer, Z. (2011). An investigation into factors which have an impact on access to and utilisation of the genetic and endoscopic surveillance clinic offered to high-risk members of known Lynch families. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/12794

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):

Bruwer, Zandré. “An investigation into factors which have an impact on access to and utilisation of the genetic and endoscopic surveillance clinic offered to high-risk members of known Lynch families.” 2011. Thesis, University of Cape Town. Accessed April 17, 2021. http://hdl.handle.net/11427/12794.

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

MLA Handbook (7th Edition):

Bruwer, Zandré. “An investigation into factors which have an impact on access to and utilisation of the genetic and endoscopic surveillance clinic offered to high-risk members of known Lynch families.” 2011. Web. 17 Apr 2021.

Vancouver:

Bruwer Z. An investigation into factors which have an impact on access to and utilisation of the genetic and endoscopic surveillance clinic offered to high-risk members of known Lynch families. [Internet] [Thesis]. University of Cape Town; 2011. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11427/12794.

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

Council of Science Editors:

Bruwer Z. An investigation into factors which have an impact on access to and utilisation of the genetic and endoscopic surveillance clinic offered to high-risk members of known Lynch families. [Thesis]. University of Cape Town; 2011. Available from: http://hdl.handle.net/11427/12794

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


University of Cape Town

11. Ruppelt, Theresa. Single nucleotide polymorphism array analysis in copy number variant detection: assessment of its feasibility in the diagnostic setting.

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

 Intellectual disability/developmental delay (ID/DD) is a significant problem in child health affecting 2 to 3% of the population worldwide. While the underlying aetiology of ID/DD… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Ruppelt, T. (2016). Single nucleotide polymorphism array analysis in copy number variant detection: assessment of its feasibility in the diagnostic setting. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/23720

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):

Ruppelt, Theresa. “Single nucleotide polymorphism array analysis in copy number variant detection: assessment of its feasibility in the diagnostic setting.” 2016. Thesis, University of Cape Town. Accessed April 17, 2021. http://hdl.handle.net/11427/23720.

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

MLA Handbook (7th Edition):

Ruppelt, Theresa. “Single nucleotide polymorphism array analysis in copy number variant detection: assessment of its feasibility in the diagnostic setting.” 2016. Web. 17 Apr 2021.

Vancouver:

Ruppelt T. Single nucleotide polymorphism array analysis in copy number variant detection: assessment of its feasibility in the diagnostic setting. [Internet] [Thesis]. University of Cape Town; 2016. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11427/23720.

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

Council of Science Editors:

Ruppelt T. Single nucleotide polymorphism array analysis in copy number variant detection: assessment of its feasibility in the diagnostic setting. [Thesis]. University of Cape Town; 2016. Available from: http://hdl.handle.net/11427/23720

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


University of Cape Town

12. Akinyi, Maureen Veronica. Functional analysis of A 5' untranslated variant in rhodopsin : implications for the retinitis pigmentosa phenotype.

Degree: Image, Division of Human Genetics, 2011, University of Cape Town

 Retinitis Pigmentosa (RP) is a group of heterogeneous retinal degenerative diseases that predominantly affect rod photoreceptor cells. Symptoms include night blindness and gradual peripheral vision… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Akinyi, M. V. (2011). Functional analysis of A 5' untranslated variant in rhodopsin : implications for the retinitis pigmentosa phenotype. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/10007

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):

Akinyi, Maureen Veronica. “Functional analysis of A 5' untranslated variant in rhodopsin : implications for the retinitis pigmentosa phenotype.” 2011. Thesis, University of Cape Town. Accessed April 17, 2021. http://hdl.handle.net/11427/10007.

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

MLA Handbook (7th Edition):

Akinyi, Maureen Veronica. “Functional analysis of A 5' untranslated variant in rhodopsin : implications for the retinitis pigmentosa phenotype.” 2011. Web. 17 Apr 2021.

Vancouver:

Akinyi MV. Functional analysis of A 5' untranslated variant in rhodopsin : implications for the retinitis pigmentosa phenotype. [Internet] [Thesis]. University of Cape Town; 2011. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11427/10007.

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

Council of Science Editors:

Akinyi MV. Functional analysis of A 5' untranslated variant in rhodopsin : implications for the retinitis pigmentosa phenotype. [Thesis]. University of Cape Town; 2011. Available from: http://hdl.handle.net/11427/10007

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


University of Cape Town

13. Naidoo, Horacia. The genetics of anthracycline-induced cardiotoxicity in cancer patients.

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

 INTRODUCTION: Breast cancer makes up 25% of all cancers diagnosed worldwide. Despite an increasing yearly incidence, there has been a significant decrease in mortality owing… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Naidoo, H. (2018). The genetics of anthracycline-induced cardiotoxicity in cancer patients. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/27839

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):

Naidoo, Horacia. “The genetics of anthracycline-induced cardiotoxicity in cancer patients.” 2018. Thesis, University of Cape Town. Accessed April 17, 2021. http://hdl.handle.net/11427/27839.

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

MLA Handbook (7th Edition):

Naidoo, Horacia. “The genetics of anthracycline-induced cardiotoxicity in cancer patients.” 2018. Web. 17 Apr 2021.

Vancouver:

Naidoo H. The genetics of anthracycline-induced cardiotoxicity in cancer patients. [Internet] [Thesis]. University of Cape Town; 2018. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11427/27839.

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

Council of Science Editors:

Naidoo H. The genetics of anthracycline-induced cardiotoxicity in cancer patients. [Thesis]. University of Cape Town; 2018. Available from: http://hdl.handle.net/11427/27839

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


University of Cape Town

14. Mhandire, Kudakwashe. Virus restriction gene variants and their possible role in neurocognitive function in children born to HIV-infected mothers.

Degree: Image, Division of Human Genetics, 2012, University of Cape Town

 Host genetic variation is an important determinant of HIV infection, disease progression and HIV-associated neurocognitive deficits. However, there is no sufficient knowledge on the role… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Mhandire, K. (2012). Virus restriction gene variants and their possible role in neurocognitive function in children born to HIV-infected mothers. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/3100

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):

Mhandire, Kudakwashe. “Virus restriction gene variants and their possible role in neurocognitive function in children born to HIV-infected mothers.” 2012. Thesis, University of Cape Town. Accessed April 17, 2021. http://hdl.handle.net/11427/3100.

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

MLA Handbook (7th Edition):

Mhandire, Kudakwashe. “Virus restriction gene variants and their possible role in neurocognitive function in children born to HIV-infected mothers.” 2012. Web. 17 Apr 2021.

Vancouver:

Mhandire K. Virus restriction gene variants and their possible role in neurocognitive function in children born to HIV-infected mothers. [Internet] [Thesis]. University of Cape Town; 2012. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11427/3100.

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

Council of Science Editors:

Mhandire K. Virus restriction gene variants and their possible role in neurocognitive function in children born to HIV-infected mothers. [Thesis]. University of Cape Town; 2012. Available from: http://hdl.handle.net/11427/3100

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


University of Cape Town

15. Berkowitz, Danielle Claire. Development of a SCA7 patient-derived lymphoblast cell model for testing RNAi knock-down of the disease-causing gene.

Degree: Image, Division of Human Genetics, 2011, University of Cape Town

 Spinocerebellar ataxia type 7 (SCA7) is an inherited neurodegenerative disease caused by the expansion of a CAG repeat within the ataxin-7 gene. The South African… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Berkowitz, D. C. (2011). Development of a SCA7 patient-derived lymphoblast cell model for testing RNAi knock-down of the disease-causing gene. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/10123

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):

Berkowitz, Danielle Claire. “Development of a SCA7 patient-derived lymphoblast cell model for testing RNAi knock-down of the disease-causing gene.” 2011. Thesis, University of Cape Town. Accessed April 17, 2021. http://hdl.handle.net/11427/10123.

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

MLA Handbook (7th Edition):

Berkowitz, Danielle Claire. “Development of a SCA7 patient-derived lymphoblast cell model for testing RNAi knock-down of the disease-causing gene.” 2011. Web. 17 Apr 2021.

Vancouver:

Berkowitz DC. Development of a SCA7 patient-derived lymphoblast cell model for testing RNAi knock-down of the disease-causing gene. [Internet] [Thesis]. University of Cape Town; 2011. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11427/10123.

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

Council of Science Editors:

Berkowitz DC. Development of a SCA7 patient-derived lymphoblast cell model for testing RNAi knock-down of the disease-causing gene. [Thesis]. University of Cape Town; 2011. Available from: http://hdl.handle.net/11427/10123

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


University of Cape Town

16. Masekoameng, Tshepiso. Sickle cell trait and targeted genomic variants in chronic kidney disease an African cohort.

Degree: MSc, Division of Human Genetics, 2019, University of Cape Town

 Background Chronic Kidney Disease (CKD), has a high and increasing burden in sub-Saharan Africa. Environmental factors that have been associated to CKD are associated with… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Masekoameng, T. (2019). Sickle cell trait and targeted genomic variants in chronic kidney disease an African cohort. (Masters Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/31357

Chicago Manual of Style (16th Edition):

Masekoameng, Tshepiso. “Sickle cell trait and targeted genomic variants in chronic kidney disease an African cohort.” 2019. Masters Thesis, University of Cape Town. Accessed April 17, 2021. http://hdl.handle.net/11427/31357.

MLA Handbook (7th Edition):

Masekoameng, Tshepiso. “Sickle cell trait and targeted genomic variants in chronic kidney disease an African cohort.” 2019. Web. 17 Apr 2021.

Vancouver:

Masekoameng T. Sickle cell trait and targeted genomic variants in chronic kidney disease an African cohort. [Internet] [Masters thesis]. University of Cape Town; 2019. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11427/31357.

Council of Science Editors:

Masekoameng T. Sickle cell trait and targeted genomic variants in chronic kidney disease an African cohort. [Masters Thesis]. University of Cape Town; 2019. Available from: http://hdl.handle.net/11427/31357


University of Cape Town

17. Rumaney, Maryam. Sickle cell anaemia in Cameroon : co-inheritance of α-thalassemia, HBB gene haplotypes, clinical & haematological characterisations.

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

 Background: Although sickle cell anaemia (SCA) is genetically characterised by a single point mutation, patients can manifest varying degrees of clinical severity due to various… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Rumaney, M. (2015). Sickle cell anaemia in Cameroon : co-inheritance of α-thalassemia, HBB gene haplotypes, clinical & haematological characterisations. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/15697

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):

Rumaney, Maryam. “Sickle cell anaemia in Cameroon : co-inheritance of α-thalassemia, HBB gene haplotypes, clinical & haematological characterisations.” 2015. Thesis, University of Cape Town. Accessed April 17, 2021. http://hdl.handle.net/11427/15697.

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

MLA Handbook (7th Edition):

Rumaney, Maryam. “Sickle cell anaemia in Cameroon : co-inheritance of α-thalassemia, HBB gene haplotypes, clinical & haematological characterisations.” 2015. Web. 17 Apr 2021.

Vancouver:

Rumaney M. Sickle cell anaemia in Cameroon : co-inheritance of α-thalassemia, HBB gene haplotypes, clinical & haematological characterisations. [Internet] [Thesis]. University of Cape Town; 2015. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11427/15697.

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

Council of Science Editors:

Rumaney M. Sickle cell anaemia in Cameroon : co-inheritance of α-thalassemia, HBB gene haplotypes, clinical & haematological characterisations. [Thesis]. University of Cape Town; 2015. Available from: http://hdl.handle.net/11427/15697

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


McGill University

18. Fotopoulos, Nellie. Brain morphology in children with ADHD: Investigating the effects of medication, candidate genes and prenatal smoking exposure.

Degree: PhD, Department of Human Genetics, 2020, McGill University

 Attention deficit/hyperactivity disorder (ADHD) is a prevalent neurodevelopmental disorder with heterogeneous clinical expression. Symptoms consist of age-inappropriate levels of inattention, hyperactivity and impulsivity beginning in… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Fotopoulos, N. (2020). Brain morphology in children with ADHD: Investigating the effects of medication, candidate genes and prenatal smoking exposure. (Doctoral Dissertation). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/sx61dr67d.pdf ; https://escholarship.mcgill.ca/concern/theses/qf85ng88f

Chicago Manual of Style (16th Edition):

Fotopoulos, Nellie. “Brain morphology in children with ADHD: Investigating the effects of medication, candidate genes and prenatal smoking exposure.” 2020. Doctoral Dissertation, McGill University. Accessed April 17, 2021. https://escholarship.mcgill.ca/downloads/sx61dr67d.pdf ; https://escholarship.mcgill.ca/concern/theses/qf85ng88f.

MLA Handbook (7th Edition):

Fotopoulos, Nellie. “Brain morphology in children with ADHD: Investigating the effects of medication, candidate genes and prenatal smoking exposure.” 2020. Web. 17 Apr 2021.

Vancouver:

Fotopoulos N. Brain morphology in children with ADHD: Investigating the effects of medication, candidate genes and prenatal smoking exposure. [Internet] [Doctoral dissertation]. McGill University; 2020. [cited 2021 Apr 17]. Available from: https://escholarship.mcgill.ca/downloads/sx61dr67d.pdf ; https://escholarship.mcgill.ca/concern/theses/qf85ng88f.

Council of Science Editors:

Fotopoulos N. Brain morphology in children with ADHD: Investigating the effects of medication, candidate genes and prenatal smoking exposure. [Doctoral Dissertation]. McGill University; 2020. Available from: https://escholarship.mcgill.ca/downloads/sx61dr67d.pdf ; https://escholarship.mcgill.ca/concern/theses/qf85ng88f


McGill University

19. Rudakou, Uladzislau. A closer look into Parkinson’s Disease GWAS genes: targeted next-generation sequencing approach.

Degree: MS, Department of Human Genetics, 2020, McGill University

 La maladie de Parkinson (MP) est la seconde maladie neurodégénérative la plus commune. Elle affecte plus de 10 millions de personnes dans le monde. L’impact… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Rudakou, U. (2020). A closer look into Parkinson’s Disease GWAS genes: targeted next-generation sequencing approach. (Masters Thesis). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/w6634806b.pdf ; https://escholarship.mcgill.ca/concern/theses/mc87pv96m

Chicago Manual of Style (16th Edition):

Rudakou, Uladzislau. “A closer look into Parkinson’s Disease GWAS genes: targeted next-generation sequencing approach.” 2020. Masters Thesis, McGill University. Accessed April 17, 2021. https://escholarship.mcgill.ca/downloads/w6634806b.pdf ; https://escholarship.mcgill.ca/concern/theses/mc87pv96m.

MLA Handbook (7th Edition):

Rudakou, Uladzislau. “A closer look into Parkinson’s Disease GWAS genes: targeted next-generation sequencing approach.” 2020. Web. 17 Apr 2021.

Vancouver:

Rudakou U. A closer look into Parkinson’s Disease GWAS genes: targeted next-generation sequencing approach. [Internet] [Masters thesis]. McGill University; 2020. [cited 2021 Apr 17]. Available from: https://escholarship.mcgill.ca/downloads/w6634806b.pdf ; https://escholarship.mcgill.ca/concern/theses/mc87pv96m.

Council of Science Editors:

Rudakou U. A closer look into Parkinson’s Disease GWAS genes: targeted next-generation sequencing approach. [Masters Thesis]. McGill University; 2020. Available from: https://escholarship.mcgill.ca/downloads/w6634806b.pdf ; https://escholarship.mcgill.ca/concern/theses/mc87pv96m


McGill University

20. Kim, Jamie. Functional characterization of Fam49b in T cells during «Salmonella» infection.

Degree: MS, Department of Human Genetics, 2020, McGill University

Salmonellae are motile, Gram-negative bacteria commonly transmitted through the ingestion of contaminated food and water. They can infect a broad range of hosts causing diseases… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Kim, J. (2020). Functional characterization of Fam49b in T cells during «Salmonella» infection. (Masters Thesis). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/ng451p06p.pdf ; https://escholarship.mcgill.ca/concern/theses/44558j75c

Chicago Manual of Style (16th Edition):

Kim, Jamie. “Functional characterization of Fam49b in T cells during «Salmonella» infection.” 2020. Masters Thesis, McGill University. Accessed April 17, 2021. https://escholarship.mcgill.ca/downloads/ng451p06p.pdf ; https://escholarship.mcgill.ca/concern/theses/44558j75c.

MLA Handbook (7th Edition):

Kim, Jamie. “Functional characterization of Fam49b in T cells during «Salmonella» infection.” 2020. Web. 17 Apr 2021.

Vancouver:

Kim J. Functional characterization of Fam49b in T cells during «Salmonella» infection. [Internet] [Masters thesis]. McGill University; 2020. [cited 2021 Apr 17]. Available from: https://escholarship.mcgill.ca/downloads/ng451p06p.pdf ; https://escholarship.mcgill.ca/concern/theses/44558j75c.

Council of Science Editors:

Kim J. Functional characterization of Fam49b in T cells during «Salmonella» infection. [Masters Thesis]. McGill University; 2020. Available from: https://escholarship.mcgill.ca/downloads/ng451p06p.pdf ; https://escholarship.mcgill.ca/concern/theses/44558j75c


McGill University

21. Hariri, Hadla. Identification of novel target genes of the parathyroid hormone-activated NACA transcriptional coregulator in bone.

Degree: PhD, Department of Human Genetics, 2020, McGill University

L'injection quotidienne d'hormone parathyroïdienne (PTH) augmente la masse osseuse etprotège contre les fractures ostéoporotiques. Cependant, le mécanisme d’action n’est pascomplètement élucidé. Nous avons démontré que… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Hariri, H. (2020). Identification of novel target genes of the parathyroid hormone-activated NACA transcriptional coregulator in bone. (Doctoral Dissertation). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/ff365967k.pdf ; https://escholarship.mcgill.ca/concern/theses/jh343x38g

Chicago Manual of Style (16th Edition):

Hariri, Hadla. “Identification of novel target genes of the parathyroid hormone-activated NACA transcriptional coregulator in bone.” 2020. Doctoral Dissertation, McGill University. Accessed April 17, 2021. https://escholarship.mcgill.ca/downloads/ff365967k.pdf ; https://escholarship.mcgill.ca/concern/theses/jh343x38g.

MLA Handbook (7th Edition):

Hariri, Hadla. “Identification of novel target genes of the parathyroid hormone-activated NACA transcriptional coregulator in bone.” 2020. Web. 17 Apr 2021.

Vancouver:

Hariri H. Identification of novel target genes of the parathyroid hormone-activated NACA transcriptional coregulator in bone. [Internet] [Doctoral dissertation]. McGill University; 2020. [cited 2021 Apr 17]. Available from: https://escholarship.mcgill.ca/downloads/ff365967k.pdf ; https://escholarship.mcgill.ca/concern/theses/jh343x38g.

Council of Science Editors:

Hariri H. Identification of novel target genes of the parathyroid hormone-activated NACA transcriptional coregulator in bone. [Doctoral Dissertation]. McGill University; 2020. Available from: https://escholarship.mcgill.ca/downloads/ff365967k.pdf ; https://escholarship.mcgill.ca/concern/theses/jh343x38g


McGill University

22. Farhangdoost, Nargess. Epigenome dysregulation resulting from NSD1 mutation in head and neck squamous cell carcinoma.

Degree: MS, Department of Human Genetics, 2020, McGill University

L'épigénétique, l'étude des changements héréditaires dans l'expression des gènes qui ne sont pas provoqués par des altérations de la séquence d'ADN, est un domaine en… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Farhangdoost, N. (2020). Epigenome dysregulation resulting from NSD1 mutation in head and neck squamous cell carcinoma. (Masters Thesis). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/7d278z992.pdf ; https://escholarship.mcgill.ca/concern/theses/xk81jr257

Chicago Manual of Style (16th Edition):

Farhangdoost, Nargess. “Epigenome dysregulation resulting from NSD1 mutation in head and neck squamous cell carcinoma.” 2020. Masters Thesis, McGill University. Accessed April 17, 2021. https://escholarship.mcgill.ca/downloads/7d278z992.pdf ; https://escholarship.mcgill.ca/concern/theses/xk81jr257.

MLA Handbook (7th Edition):

Farhangdoost, Nargess. “Epigenome dysregulation resulting from NSD1 mutation in head and neck squamous cell carcinoma.” 2020. Web. 17 Apr 2021.

Vancouver:

Farhangdoost N. Epigenome dysregulation resulting from NSD1 mutation in head and neck squamous cell carcinoma. [Internet] [Masters thesis]. McGill University; 2020. [cited 2021 Apr 17]. Available from: https://escholarship.mcgill.ca/downloads/7d278z992.pdf ; https://escholarship.mcgill.ca/concern/theses/xk81jr257.

Council of Science Editors:

Farhangdoost N. Epigenome dysregulation resulting from NSD1 mutation in head and neck squamous cell carcinoma. [Masters Thesis]. McGill University; 2020. Available from: https://escholarship.mcgill.ca/downloads/7d278z992.pdf ; https://escholarship.mcgill.ca/concern/theses/xk81jr257


McGill University

23. Baguette, Audrey. Characterization of the interplay between the genome architecture and gene co-expression.

Degree: MS, Department of Human Genetics, 2020, McGill University

The relation between the structure of the genome and gene regulation is critical to normal and disease development, but the molecular details of how they… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Baguette, A. (2020). Characterization of the interplay between the genome architecture and gene co-expression. (Masters Thesis). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/nz8064717.pdf ; https://escholarship.mcgill.ca/concern/theses/qj72pc78f

Chicago Manual of Style (16th Edition):

Baguette, Audrey. “Characterization of the interplay between the genome architecture and gene co-expression.” 2020. Masters Thesis, McGill University. Accessed April 17, 2021. https://escholarship.mcgill.ca/downloads/nz8064717.pdf ; https://escholarship.mcgill.ca/concern/theses/qj72pc78f.

MLA Handbook (7th Edition):

Baguette, Audrey. “Characterization of the interplay between the genome architecture and gene co-expression.” 2020. Web. 17 Apr 2021.

Vancouver:

Baguette A. Characterization of the interplay between the genome architecture and gene co-expression. [Internet] [Masters thesis]. McGill University; 2020. [cited 2021 Apr 17]. Available from: https://escholarship.mcgill.ca/downloads/nz8064717.pdf ; https://escholarship.mcgill.ca/concern/theses/qj72pc78f.

Council of Science Editors:

Baguette A. Characterization of the interplay between the genome architecture and gene co-expression. [Masters Thesis]. McGill University; 2020. Available from: https://escholarship.mcgill.ca/downloads/nz8064717.pdf ; https://escholarship.mcgill.ca/concern/theses/qj72pc78f


McGill University

24. Mufti, Kheireddin. Targeted next-generation sequencing approach to study the role of Parkinsonism genes in REM sleep behavior disorder.

Degree: MS, Department of Human Genetics, 2020, McGill University

 Isolated REM sleep behavior disorder (iRBD) is a parasomnia that is characterized by loss of muscle atonia and dream enactment during REM sleep. iRBD is,… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Mufti, K. (2020). Targeted next-generation sequencing approach to study the role of Parkinsonism genes in REM sleep behavior disorder. (Masters Thesis). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/wp988q43t.pdf ; https://escholarship.mcgill.ca/concern/theses/6d570215j

Chicago Manual of Style (16th Edition):

Mufti, Kheireddin. “Targeted next-generation sequencing approach to study the role of Parkinsonism genes in REM sleep behavior disorder.” 2020. Masters Thesis, McGill University. Accessed April 17, 2021. https://escholarship.mcgill.ca/downloads/wp988q43t.pdf ; https://escholarship.mcgill.ca/concern/theses/6d570215j.

MLA Handbook (7th Edition):

Mufti, Kheireddin. “Targeted next-generation sequencing approach to study the role of Parkinsonism genes in REM sleep behavior disorder.” 2020. Web. 17 Apr 2021.

Vancouver:

Mufti K. Targeted next-generation sequencing approach to study the role of Parkinsonism genes in REM sleep behavior disorder. [Internet] [Masters thesis]. McGill University; 2020. [cited 2021 Apr 17]. Available from: https://escholarship.mcgill.ca/downloads/wp988q43t.pdf ; https://escholarship.mcgill.ca/concern/theses/6d570215j.

Council of Science Editors:

Mufti K. Targeted next-generation sequencing approach to study the role of Parkinsonism genes in REM sleep behavior disorder. [Masters Thesis]. McGill University; 2020. Available from: https://escholarship.mcgill.ca/downloads/wp988q43t.pdf ; https://escholarship.mcgill.ca/concern/theses/6d570215j


McGill University

25. Karam, Nabila. MYF6-mediated muscle-bone cross-talk and its effect on bone remodelling.

Degree: MS, Department of Human Genetics, 2020, McGill University

Outre sa capacité à fournir de la force physique et à générer de l'énergie, le muscle s'est également adapté pour être un organe endocrinien qui… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Karam, N. (2020). MYF6-mediated muscle-bone cross-talk and its effect on bone remodelling. (Masters Thesis). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/fj2366968.pdf ; https://escholarship.mcgill.ca/concern/theses/pk02cg326

Chicago Manual of Style (16th Edition):

Karam, Nabila. “MYF6-mediated muscle-bone cross-talk and its effect on bone remodelling.” 2020. Masters Thesis, McGill University. Accessed April 17, 2021. https://escholarship.mcgill.ca/downloads/fj2366968.pdf ; https://escholarship.mcgill.ca/concern/theses/pk02cg326.

MLA Handbook (7th Edition):

Karam, Nabila. “MYF6-mediated muscle-bone cross-talk and its effect on bone remodelling.” 2020. Web. 17 Apr 2021.

Vancouver:

Karam N. MYF6-mediated muscle-bone cross-talk and its effect on bone remodelling. [Internet] [Masters thesis]. McGill University; 2020. [cited 2021 Apr 17]. Available from: https://escholarship.mcgill.ca/downloads/fj2366968.pdf ; https://escholarship.mcgill.ca/concern/theses/pk02cg326.

Council of Science Editors:

Karam N. MYF6-mediated muscle-bone cross-talk and its effect on bone remodelling. [Masters Thesis]. McGill University; 2020. Available from: https://escholarship.mcgill.ca/downloads/fj2366968.pdf ; https://escholarship.mcgill.ca/concern/theses/pk02cg326


McGill University

26. Tahir, Maryam. The impact of maternal genetic and dietary disturbances in one-carbon metabolism on embryonic development.

Degree: MS, Department of Human Genetics, 2020, McGill University

 The vitamin folate is involved in one-carbon metabolism and the remethylation of homocysteine to methionine. Disturbances in folate metabolism can result in an increased risk… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Tahir, M. (2020). The impact of maternal genetic and dietary disturbances in one-carbon metabolism on embryonic development. (Masters Thesis). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/8623j3672.pdf ; https://escholarship.mcgill.ca/concern/theses/028711629

Chicago Manual of Style (16th Edition):

Tahir, Maryam. “The impact of maternal genetic and dietary disturbances in one-carbon metabolism on embryonic development.” 2020. Masters Thesis, McGill University. Accessed April 17, 2021. https://escholarship.mcgill.ca/downloads/8623j3672.pdf ; https://escholarship.mcgill.ca/concern/theses/028711629.

MLA Handbook (7th Edition):

Tahir, Maryam. “The impact of maternal genetic and dietary disturbances in one-carbon metabolism on embryonic development.” 2020. Web. 17 Apr 2021.

Vancouver:

Tahir M. The impact of maternal genetic and dietary disturbances in one-carbon metabolism on embryonic development. [Internet] [Masters thesis]. McGill University; 2020. [cited 2021 Apr 17]. Available from: https://escholarship.mcgill.ca/downloads/8623j3672.pdf ; https://escholarship.mcgill.ca/concern/theses/028711629.

Council of Science Editors:

Tahir M. The impact of maternal genetic and dietary disturbances in one-carbon metabolism on embryonic development. [Masters Thesis]. McGill University; 2020. Available from: https://escholarship.mcgill.ca/downloads/8623j3672.pdf ; https://escholarship.mcgill.ca/concern/theses/028711629


McGill University

27. Manzano Vargas, Karla. Induced pluripotent stem cell models of Kleefstra syndrome.

Degree: MS, Department of Human Genetics, 2019, McGill University

Le syndrome de Kleefstra (SK) est un trouble neuro-développemental principalement caractérisé par un déficit intellectuel, une dysmorphie faciale caractéristique et une hypotonie infantile. Le SK… (more)

Subjects/Keywords: Human Genetics

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APA (6th Edition):

Manzano Vargas, K. (2019). Induced pluripotent stem cell models of Kleefstra syndrome. (Masters Thesis). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/kh04dr828.pdf ; https://escholarship.mcgill.ca/concern/theses/5712m907x

Chicago Manual of Style (16th Edition):

Manzano Vargas, Karla. “Induced pluripotent stem cell models of Kleefstra syndrome.” 2019. Masters Thesis, McGill University. Accessed April 17, 2021. https://escholarship.mcgill.ca/downloads/kh04dr828.pdf ; https://escholarship.mcgill.ca/concern/theses/5712m907x.

MLA Handbook (7th Edition):

Manzano Vargas, Karla. “Induced pluripotent stem cell models of Kleefstra syndrome.” 2019. Web. 17 Apr 2021.

Vancouver:

Manzano Vargas K. Induced pluripotent stem cell models of Kleefstra syndrome. [Internet] [Masters thesis]. McGill University; 2019. [cited 2021 Apr 17]. Available from: https://escholarship.mcgill.ca/downloads/kh04dr828.pdf ; https://escholarship.mcgill.ca/concern/theses/5712m907x.

Council of Science Editors:

Manzano Vargas K. Induced pluripotent stem cell models of Kleefstra syndrome. [Masters Thesis]. McGill University; 2019. Available from: https://escholarship.mcgill.ca/downloads/kh04dr828.pdf ; https://escholarship.mcgill.ca/concern/theses/5712m907x


University of Cape Town

28. Geard, Amy. Association of variants in APOL1, MYH9 and HMOX1 WITH micro-Albuminuria among Sickle Cell disease patients from Cameroon.

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

 Introduction: Sickle Cell Disease (SCD) is a monogenic, multi-organ hemoglobinopathy disorder that is highly prevalent in Africa, with nearly 300 000 newborn cases per year.… (more)

Subjects/Keywords: Human Genetics

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

APA (6th Edition):

Geard, A. (2016). Association of variants in APOL1, MYH9 and HMOX1 WITH micro-Albuminuria among Sickle Cell disease patients from Cameroon. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/23042

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):

Geard, Amy. “Association of variants in APOL1, MYH9 and HMOX1 WITH micro-Albuminuria among Sickle Cell disease patients from Cameroon.” 2016. Thesis, University of Cape Town. Accessed April 17, 2021. http://hdl.handle.net/11427/23042.

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

MLA Handbook (7th Edition):

Geard, Amy. “Association of variants in APOL1, MYH9 and HMOX1 WITH micro-Albuminuria among Sickle Cell disease patients from Cameroon.” 2016. Web. 17 Apr 2021.

Vancouver:

Geard A. Association of variants in APOL1, MYH9 and HMOX1 WITH micro-Albuminuria among Sickle Cell disease patients from Cameroon. [Internet] [Thesis]. University of Cape Town; 2016. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11427/23042.

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

Council of Science Editors:

Geard A. Association of variants in APOL1, MYH9 and HMOX1 WITH micro-Albuminuria among Sickle Cell disease patients from Cameroon. [Thesis]. University of Cape Town; 2016. Available from: http://hdl.handle.net/11427/23042

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


Euskal Herriko Unibertsitatea / Universidad del País Vasco

29. Martínez de la Piscina Martín, Idoia. Clinical and molecular characterization of DSD patients: Impact of Next Generation Sequencing in diagnosis .

Degree: 2020, Euskal Herriko Unibertsitatea / Universidad del País Vasco

 Disorders of sex development (DSD) encompass a high heterogeneous range of conditionsin which the optimal clinical management of the individuals comprise clinical description, biochemicaltesting and… (more)

Subjects/Keywords: human genetics

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

APA (6th Edition):

Martínez de la Piscina Martín, I. (2020). Clinical and molecular characterization of DSD patients: Impact of Next Generation Sequencing in diagnosis . (Doctoral Dissertation). Euskal Herriko Unibertsitatea / Universidad del País Vasco. Retrieved from http://hdl.handle.net/10810/50270

Chicago Manual of Style (16th Edition):

Martínez de la Piscina Martín, Idoia. “Clinical and molecular characterization of DSD patients: Impact of Next Generation Sequencing in diagnosis .” 2020. Doctoral Dissertation, Euskal Herriko Unibertsitatea / Universidad del País Vasco. Accessed April 17, 2021. http://hdl.handle.net/10810/50270.

MLA Handbook (7th Edition):

Martínez de la Piscina Martín, Idoia. “Clinical and molecular characterization of DSD patients: Impact of Next Generation Sequencing in diagnosis .” 2020. Web. 17 Apr 2021.

Vancouver:

Martínez de la Piscina Martín I. Clinical and molecular characterization of DSD patients: Impact of Next Generation Sequencing in diagnosis . [Internet] [Doctoral dissertation]. Euskal Herriko Unibertsitatea / Universidad del País Vasco; 2020. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/10810/50270.

Council of Science Editors:

Martínez de la Piscina Martín I. Clinical and molecular characterization of DSD patients: Impact of Next Generation Sequencing in diagnosis . [Doctoral Dissertation]. Euskal Herriko Unibertsitatea / Universidad del País Vasco; 2020. Available from: http://hdl.handle.net/10810/50270


University of Cape Town

30. Baine, Fiona Eugenie Kebirungi. A molecular investigation of Huntington disease; origins of the mutation and current prevalence in South Africa.

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

 Huntington disease (HD) is a devastating neurodegenerative condition characterised by a triad of symptoms: behavioural/psychiatric changes, cognitive decline and movement disorder. The dominantly inherited disease-causing… (more)

Subjects/Keywords: Human Genetics

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

APA (6th Edition):

Baine, F. E. K. (2015). A molecular investigation of Huntington disease; origins of the mutation and current prevalence in South Africa. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/20260

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):

Baine, Fiona Eugenie Kebirungi. “A molecular investigation of Huntington disease; origins of the mutation and current prevalence in South Africa.” 2015. Thesis, University of Cape Town. Accessed April 17, 2021. http://hdl.handle.net/11427/20260.

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

MLA Handbook (7th Edition):

Baine, Fiona Eugenie Kebirungi. “A molecular investigation of Huntington disease; origins of the mutation and current prevalence in South Africa.” 2015. Web. 17 Apr 2021.

Vancouver:

Baine FEK. A molecular investigation of Huntington disease; origins of the mutation and current prevalence in South Africa. [Internet] [Thesis]. University of Cape Town; 2015. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11427/20260.

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

Council of Science Editors:

Baine FEK. A molecular investigation of Huntington disease; origins of the mutation and current prevalence in South Africa. [Thesis]. University of Cape Town; 2015. Available from: http://hdl.handle.net/11427/20260

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

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