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You searched for subject:(Medical genetics). Showing records 1 – 30 of 636 total matches.

[1] [2] [3] [4] [5] … [22]

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University of Helsinki

1. Vlachopoulou, Efthymia. HLA-DRB1: Haplotype Diversity, Imputation and Association with Acute Coronary Syndrome.

Degree: Haartman Institute, 2015, University of Helsinki

The Human Leukocyte Antigen (HLA) region is located on chromosome 6 (6p21.3) and its main function is to regulate the immune system. This region has… (more)

Subjects/Keywords: Medical Genetics; Medical Genetics

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APA (6th Edition):

Vlachopoulou, E. (2015). HLA-DRB1: Haplotype Diversity, Imputation and Association with Acute Coronary Syndrome. (Doctoral Dissertation). University of Helsinki. Retrieved from http://hdl.handle.net/10138/156247

Chicago Manual of Style (16th Edition):

Vlachopoulou, Efthymia. “HLA-DRB1: Haplotype Diversity, Imputation and Association with Acute Coronary Syndrome.” 2015. Doctoral Dissertation, University of Helsinki. Accessed September 17, 2019. http://hdl.handle.net/10138/156247.

MLA Handbook (7th Edition):

Vlachopoulou, Efthymia. “HLA-DRB1: Haplotype Diversity, Imputation and Association with Acute Coronary Syndrome.” 2015. Web. 17 Sep 2019.

Vancouver:

Vlachopoulou E. HLA-DRB1: Haplotype Diversity, Imputation and Association with Acute Coronary Syndrome. [Internet] [Doctoral dissertation]. University of Helsinki; 2015. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/10138/156247.

Council of Science Editors:

Vlachopoulou E. HLA-DRB1: Haplotype Diversity, Imputation and Association with Acute Coronary Syndrome. [Doctoral Dissertation]. University of Helsinki; 2015. Available from: http://hdl.handle.net/10138/156247


University of Cape Town

2. Ngongang Tekendo, Cedrik. Genetic investigation of South Africans with the Noonan Syndrome phenotype using targeted next generation sequencing.

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

 Introduction: Noonan Syndrome (NS) is an autosomal dominant multisystem disorder, characterised by short stature, distinctive facial dysmorphism, cardiovascular abnormalities and developmental delay. Its estimated incidence… (more)

Subjects/Keywords: Medical Genetics

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APA (6th Edition):

Ngongang Tekendo, C. (2017). Genetic investigation of South Africans with the Noonan Syndrome phenotype using targeted next generation sequencing. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/27376

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):

Ngongang Tekendo, Cedrik. “Genetic investigation of South Africans with the Noonan Syndrome phenotype using targeted next generation sequencing.” 2017. Thesis, University of Cape Town. Accessed September 17, 2019. http://hdl.handle.net/11427/27376.

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

MLA Handbook (7th Edition):

Ngongang Tekendo, Cedrik. “Genetic investigation of South Africans with the Noonan Syndrome phenotype using targeted next generation sequencing.” 2017. Web. 17 Sep 2019.

Vancouver:

Ngongang Tekendo C. Genetic investigation of South Africans with the Noonan Syndrome phenotype using targeted next generation sequencing. [Internet] [Thesis]. University of Cape Town; 2017. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/11427/27376.

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

Council of Science Editors:

Ngongang Tekendo C. Genetic investigation of South Africans with the Noonan Syndrome phenotype using targeted next generation sequencing. [Thesis]. University of Cape Town; 2017. Available from: http://hdl.handle.net/11427/27376

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


Virginia Commonwealth University

3. Peterson, Kristen N. Investigating the Role of Bptf in Immunoediting in Breast Cancer and Melanoma.

Degree: MS, Human Genetics, 2015, Virginia Commonwealth University

  In this study, we explore the effects of NURF depletion on the growth of tumors in immune-competent mice. NURF depletion in tumors results in… (more)

Subjects/Keywords: Medical Genetics

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APA (6th Edition):

Peterson, K. N. (2015). Investigating the Role of Bptf in Immunoediting in Breast Cancer and Melanoma. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/3793

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):

Peterson, Kristen N. “Investigating the Role of Bptf in Immunoediting in Breast Cancer and Melanoma.” 2015. Thesis, Virginia Commonwealth University. Accessed September 17, 2019. https://scholarscompass.vcu.edu/etd/3793.

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

MLA Handbook (7th Edition):

Peterson, Kristen N. “Investigating the Role of Bptf in Immunoediting in Breast Cancer and Melanoma.” 2015. Web. 17 Sep 2019.

Vancouver:

Peterson KN. Investigating the Role of Bptf in Immunoediting in Breast Cancer and Melanoma. [Internet] [Thesis]. Virginia Commonwealth University; 2015. [cited 2019 Sep 17]. Available from: https://scholarscompass.vcu.edu/etd/3793.

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

Council of Science Editors:

Peterson KN. Investigating the Role of Bptf in Immunoediting in Breast Cancer and Melanoma. [Thesis]. Virginia Commonwealth University; 2015. Available from: https://scholarscompass.vcu.edu/etd/3793

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


University of Central Florida

4. Hassouneh, Sayf Al-Deen. Role of Mycobacterium avium paratuberculosis (MAP) and TNFSF15 SNPs on TL1A in CD.

Degree: 2018, University of Central Florida

 Tumor Necrosis Factor-Like Ligand 1a (TL1A) is a cytokine encoded by Tumor Necrosis Factor Super Family 15 gene (TNFSF15) gene mostly in endothelial cells which… (more)

Subjects/Keywords: Medical Biotechnology; Medical Genetics

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APA (6th Edition):

Hassouneh, S. A. (2018). Role of Mycobacterium avium paratuberculosis (MAP) and TNFSF15 SNPs on TL1A in CD. (Masters Thesis). University of Central Florida. Retrieved from https://stars.library.ucf.edu/etd/5947

Chicago Manual of Style (16th Edition):

Hassouneh, Sayf Al-Deen. “Role of Mycobacterium avium paratuberculosis (MAP) and TNFSF15 SNPs on TL1A in CD.” 2018. Masters Thesis, University of Central Florida. Accessed September 17, 2019. https://stars.library.ucf.edu/etd/5947.

MLA Handbook (7th Edition):

Hassouneh, Sayf Al-Deen. “Role of Mycobacterium avium paratuberculosis (MAP) and TNFSF15 SNPs on TL1A in CD.” 2018. Web. 17 Sep 2019.

Vancouver:

Hassouneh SA. Role of Mycobacterium avium paratuberculosis (MAP) and TNFSF15 SNPs on TL1A in CD. [Internet] [Masters thesis]. University of Central Florida; 2018. [cited 2019 Sep 17]. Available from: https://stars.library.ucf.edu/etd/5947.

Council of Science Editors:

Hassouneh SA. Role of Mycobacterium avium paratuberculosis (MAP) and TNFSF15 SNPs on TL1A in CD. [Masters Thesis]. University of Central Florida; 2018. Available from: https://stars.library.ucf.edu/etd/5947


McMaster University

5. Beatty, Laura. Adiponectin Receptor 1 and Liver Kinase B1 are Downregulated in Renal Cell Carcinoma.

Degree: MSMS, 2011, McMaster University

Obesity is the latest epidemic of the 21st century. Indeed, numerous studies have associated obesity with an increased risk of developing several health conditions,… (more)

Subjects/Keywords: AdipoR1; LKB1; RCC; Medical Genetics; Medical Genetics

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APA (6th Edition):

Beatty, L. (2011). Adiponectin Receptor 1 and Liver Kinase B1 are Downregulated in Renal Cell Carcinoma. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/11350

Chicago Manual of Style (16th Edition):

Beatty, Laura. “Adiponectin Receptor 1 and Liver Kinase B1 are Downregulated in Renal Cell Carcinoma.” 2011. Masters Thesis, McMaster University. Accessed September 17, 2019. http://hdl.handle.net/11375/11350.

MLA Handbook (7th Edition):

Beatty, Laura. “Adiponectin Receptor 1 and Liver Kinase B1 are Downregulated in Renal Cell Carcinoma.” 2011. Web. 17 Sep 2019.

Vancouver:

Beatty L. Adiponectin Receptor 1 and Liver Kinase B1 are Downregulated in Renal Cell Carcinoma. [Internet] [Masters thesis]. McMaster University; 2011. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/11375/11350.

Council of Science Editors:

Beatty L. Adiponectin Receptor 1 and Liver Kinase B1 are Downregulated in Renal Cell Carcinoma. [Masters Thesis]. McMaster University; 2011. Available from: http://hdl.handle.net/11375/11350

6. Pithara, Christalla. Identifying the benefits and disbenefits of clinical genetics services : a framework for economic evaluation.

Degree: PhD, University of Glamorgan, 2012, University of South Wales

 A number of methodological considerations have been discussed in the area of economic evaluation of Clinical Genetic Services (CGSs) including the limited knowledge of psychosocial… (more)

Subjects/Keywords: Medical genetics; 616.042

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APA (6th Edition):

Pithara, C. (2012). Identifying the benefits and disbenefits of clinical genetics services : a framework for economic evaluation. (Doctoral Dissertation). University of South Wales. Retrieved from http://hdl.handle.net/10265/563

Chicago Manual of Style (16th Edition):

Pithara, Christalla. “Identifying the benefits and disbenefits of clinical genetics services : a framework for economic evaluation.” 2012. Doctoral Dissertation, University of South Wales. Accessed September 17, 2019. http://hdl.handle.net/10265/563.

MLA Handbook (7th Edition):

Pithara, Christalla. “Identifying the benefits and disbenefits of clinical genetics services : a framework for economic evaluation.” 2012. Web. 17 Sep 2019.

Vancouver:

Pithara C. Identifying the benefits and disbenefits of clinical genetics services : a framework for economic evaluation. [Internet] [Doctoral dissertation]. University of South Wales; 2012. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/10265/563.

Council of Science Editors:

Pithara C. Identifying the benefits and disbenefits of clinical genetics services : a framework for economic evaluation. [Doctoral Dissertation]. University of South Wales; 2012. Available from: http://hdl.handle.net/10265/563

7. Pithara, Christalla. Identifying the benefits and disbenefits of clinical genetics services : a framework for economic evaluation.

Degree: PhD, 2011, University of South Wales

 A number of methodological considerations have been discussed in the area of economic evaluation of Clinical Genetic Services (CGSs) including the limited knowledge of psychosocial… (more)

Subjects/Keywords: 616.042; Medical genetics

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APA (6th Edition):

Pithara, C. (2011). Identifying the benefits and disbenefits of clinical genetics services : a framework for economic evaluation. (Doctoral Dissertation). University of South Wales. Retrieved from https://pure.southwales.ac.uk/en/studentthesis/identifying-the-benefits-and-disbenefits-of-clinical-genetics-services(26dc5692-8d18-4977-99e4-90fd8e76d0fb).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.551129

Chicago Manual of Style (16th Edition):

Pithara, Christalla. “Identifying the benefits and disbenefits of clinical genetics services : a framework for economic evaluation.” 2011. Doctoral Dissertation, University of South Wales. Accessed September 17, 2019. https://pure.southwales.ac.uk/en/studentthesis/identifying-the-benefits-and-disbenefits-of-clinical-genetics-services(26dc5692-8d18-4977-99e4-90fd8e76d0fb).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.551129.

MLA Handbook (7th Edition):

Pithara, Christalla. “Identifying the benefits and disbenefits of clinical genetics services : a framework for economic evaluation.” 2011. Web. 17 Sep 2019.

Vancouver:

Pithara C. Identifying the benefits and disbenefits of clinical genetics services : a framework for economic evaluation. [Internet] [Doctoral dissertation]. University of South Wales; 2011. [cited 2019 Sep 17]. Available from: https://pure.southwales.ac.uk/en/studentthesis/identifying-the-benefits-and-disbenefits-of-clinical-genetics-services(26dc5692-8d18-4977-99e4-90fd8e76d0fb).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.551129.

Council of Science Editors:

Pithara C. Identifying the benefits and disbenefits of clinical genetics services : a framework for economic evaluation. [Doctoral Dissertation]. University of South Wales; 2011. Available from: https://pure.southwales.ac.uk/en/studentthesis/identifying-the-benefits-and-disbenefits-of-clinical-genetics-services(26dc5692-8d18-4977-99e4-90fd8e76d0fb).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.551129


McGill University

8. Glick, Hyman. Epidemiology of microphthalmia in an inbred mouse strain.

Degree: MS, Department of Genetics, 1966, McGill University

 Within the C57BL/Fr inbred mouse strain, microphthalmia, the reduction in eyeball diameter, occurred spontaneously among 14.68% of the newborns. Microphthalmia was commoner and more severe… (more)

Subjects/Keywords: Medical genetics.; Genetics.

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APA (6th Edition):

Glick, H. (1966). Epidemiology of microphthalmia in an inbred mouse strain. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile73610.pdf

Chicago Manual of Style (16th Edition):

Glick, Hyman. “Epidemiology of microphthalmia in an inbred mouse strain.” 1966. Masters Thesis, McGill University. Accessed September 17, 2019. http://digitool.library.mcgill.ca/thesisfile73610.pdf.

MLA Handbook (7th Edition):

Glick, Hyman. “Epidemiology of microphthalmia in an inbred mouse strain.” 1966. Web. 17 Sep 2019.

Vancouver:

Glick H. Epidemiology of microphthalmia in an inbred mouse strain. [Internet] [Masters thesis]. McGill University; 1966. [cited 2019 Sep 17]. Available from: http://digitool.library.mcgill.ca/thesisfile73610.pdf.

Council of Science Editors:

Glick H. Epidemiology of microphthalmia in an inbred mouse strain. [Masters Thesis]. McGill University; 1966. Available from: http://digitool.library.mcgill.ca/thesisfile73610.pdf


University of Oxford

9. Shipman, Lydia. The functional consequences of autoimmune variants in the tyrosine kinase 2 gene region.

Degree: PhD, 2014, University of Oxford

 The tyrosine kinase 2 (TYK2) gene was first implicated in autoimmune disease in 2009 when a nonsynonymous single nucleotide polymorphism (nsSNP) in TYK2 was reported… (more)

Subjects/Keywords: 616.07; Genetics (medical sciences); Immunology; Autoimmunity; genetics

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APA (6th Edition):

Shipman, L. (2014). The functional consequences of autoimmune variants in the tyrosine kinase 2 gene region. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:d7546fb0-3eb3-459c-867f-6e83d5dc2387 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644708

Chicago Manual of Style (16th Edition):

Shipman, Lydia. “The functional consequences of autoimmune variants in the tyrosine kinase 2 gene region.” 2014. Doctoral Dissertation, University of Oxford. Accessed September 17, 2019. http://ora.ox.ac.uk/objects/uuid:d7546fb0-3eb3-459c-867f-6e83d5dc2387 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644708.

MLA Handbook (7th Edition):

Shipman, Lydia. “The functional consequences of autoimmune variants in the tyrosine kinase 2 gene region.” 2014. Web. 17 Sep 2019.

Vancouver:

Shipman L. The functional consequences of autoimmune variants in the tyrosine kinase 2 gene region. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2019 Sep 17]. Available from: http://ora.ox.ac.uk/objects/uuid:d7546fb0-3eb3-459c-867f-6e83d5dc2387 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644708.

Council of Science Editors:

Shipman L. The functional consequences of autoimmune variants in the tyrosine kinase 2 gene region. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:d7546fb0-3eb3-459c-867f-6e83d5dc2387 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644708


University of Iowa

10. Yen, Hsan-jan. Development of the zebrafish as a model for Bardet-Biedl syndrome.

Degree: PhD, Genetics, 2007, University of Iowa

  Bardet-Biedl syndrome (BBS) is an autosomal recessive disorder characterized by obesity, retinitis pigmentosa, polydactyly, mental retardation and hypogonadism. To date, twelve BBS genes have… (more)

Subjects/Keywords: Genetics; Medical Genetics

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APA (6th Edition):

Yen, H. (2007). Development of the zebrafish as a model for Bardet-Biedl syndrome. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/133

Chicago Manual of Style (16th Edition):

Yen, Hsan-jan. “Development of the zebrafish as a model for Bardet-Biedl syndrome.” 2007. Doctoral Dissertation, University of Iowa. Accessed September 17, 2019. https://ir.uiowa.edu/etd/133.

MLA Handbook (7th Edition):

Yen, Hsan-jan. “Development of the zebrafish as a model for Bardet-Biedl syndrome.” 2007. Web. 17 Sep 2019.

Vancouver:

Yen H. Development of the zebrafish as a model for Bardet-Biedl syndrome. [Internet] [Doctoral dissertation]. University of Iowa; 2007. [cited 2019 Sep 17]. Available from: https://ir.uiowa.edu/etd/133.

Council of Science Editors:

Yen H. Development of the zebrafish as a model for Bardet-Biedl syndrome. [Doctoral Dissertation]. University of Iowa; 2007. Available from: https://ir.uiowa.edu/etd/133


University of Hong Kong

11. 陈若言; Chen, Ruoyan. A new tool for detecting short inversions using next generation sequencing (NGS) data and a systematic comparison of different NGS platforms on detection sensitivities.

Degree: PhD, 2017, University of Hong Kong

Rapid development of Next Generation Sequencing (NGS) technology has substantially transformed the landscape of biomedical research. As a result, analyses based on these sequencing technologies,… (more)

Subjects/Keywords: Nucleotide sequence; Medical genetics

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APA (6th Edition):

陈若言; Chen, R. (2017). A new tool for detecting short inversions using next generation sequencing (NGS) data and a systematic comparison of different NGS platforms on detection sensitivities. (Doctoral Dissertation). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/250733

Chicago Manual of Style (16th Edition):

陈若言; Chen, Ruoyan. “A new tool for detecting short inversions using next generation sequencing (NGS) data and a systematic comparison of different NGS platforms on detection sensitivities.” 2017. Doctoral Dissertation, University of Hong Kong. Accessed September 17, 2019. http://hdl.handle.net/10722/250733.

MLA Handbook (7th Edition):

陈若言; Chen, Ruoyan. “A new tool for detecting short inversions using next generation sequencing (NGS) data and a systematic comparison of different NGS platforms on detection sensitivities.” 2017. Web. 17 Sep 2019.

Vancouver:

陈若言; Chen R. A new tool for detecting short inversions using next generation sequencing (NGS) data and a systematic comparison of different NGS platforms on detection sensitivities. [Internet] [Doctoral dissertation]. University of Hong Kong; 2017. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/10722/250733.

Council of Science Editors:

陈若言; Chen R. A new tool for detecting short inversions using next generation sequencing (NGS) data and a systematic comparison of different NGS platforms on detection sensitivities. [Doctoral Dissertation]. University of Hong Kong; 2017. Available from: http://hdl.handle.net/10722/250733


University of Hong Kong

12. Yeung, Kit-san. The use of genome-wide DNA methylation microarray to study both the common and rare diseases.

Degree: M. Phil., 2014, University of Hong Kong

 DNA methylation plays many important roles in human physiology such as imprinting and X chromosome inactivation (XCI), and therefore disruption in DNA methylation can lead… (more)

Subjects/Keywords: DNA - Methylation; Medical genetics

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APA (6th Edition):

Yeung, K. (2014). The use of genome-wide DNA methylation microarray to study both the common and rare diseases. (Masters Thesis). University of Hong Kong. Retrieved from Yeung, K. [楊傑燊]. (2014). The use of genome-wide DNA methylation microarray to study both the common and rare diseases. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5334844 ; http://dx.doi.org/10.5353/th_b5334844 ; http://hdl.handle.net/10722/220770

Chicago Manual of Style (16th Edition):

Yeung, Kit-san. “The use of genome-wide DNA methylation microarray to study both the common and rare diseases.” 2014. Masters Thesis, University of Hong Kong. Accessed September 17, 2019. Yeung, K. [楊傑燊]. (2014). The use of genome-wide DNA methylation microarray to study both the common and rare diseases. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5334844 ; http://dx.doi.org/10.5353/th_b5334844 ; http://hdl.handle.net/10722/220770.

MLA Handbook (7th Edition):

Yeung, Kit-san. “The use of genome-wide DNA methylation microarray to study both the common and rare diseases.” 2014. Web. 17 Sep 2019.

Vancouver:

Yeung K. The use of genome-wide DNA methylation microarray to study both the common and rare diseases. [Internet] [Masters thesis]. University of Hong Kong; 2014. [cited 2019 Sep 17]. Available from: Yeung, K. [楊傑燊]. (2014). The use of genome-wide DNA methylation microarray to study both the common and rare diseases. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5334844 ; http://dx.doi.org/10.5353/th_b5334844 ; http://hdl.handle.net/10722/220770.

Council of Science Editors:

Yeung K. The use of genome-wide DNA methylation microarray to study both the common and rare diseases. [Masters Thesis]. University of Hong Kong; 2014. Available from: Yeung, K. [楊傑燊]. (2014). The use of genome-wide DNA methylation microarray to study both the common and rare diseases. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5334844 ; http://dx.doi.org/10.5353/th_b5334844 ; http://hdl.handle.net/10722/220770


McGill University

13. Hunter, Alasdair Grant Walker. Studies in medical genetics.

Degree: MS, Department of Genetics, 1971, McGill University

Subjects/Keywords: Medical genetics.

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APA (6th Edition):

Hunter, A. G. W. (1971). Studies in medical genetics. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile47744.pdf

Chicago Manual of Style (16th Edition):

Hunter, Alasdair Grant Walker. “Studies in medical genetics.” 1971. Masters Thesis, McGill University. Accessed September 17, 2019. http://digitool.library.mcgill.ca/thesisfile47744.pdf.

MLA Handbook (7th Edition):

Hunter, Alasdair Grant Walker. “Studies in medical genetics.” 1971. Web. 17 Sep 2019.

Vancouver:

Hunter AGW. Studies in medical genetics. [Internet] [Masters thesis]. McGill University; 1971. [cited 2019 Sep 17]. Available from: http://digitool.library.mcgill.ca/thesisfile47744.pdf.

Council of Science Editors:

Hunter AGW. Studies in medical genetics. [Masters Thesis]. McGill University; 1971. Available from: http://digitool.library.mcgill.ca/thesisfile47744.pdf


Columbia University

14. Kuo, Chao-Ling. Characterization ofAthsq1, an Atherosclerosis Modifier Locus on Mouse Chromosome 4:.

Degree: 2011, Columbia University

 Atherosclerosis, the primary cause of heart attack, stroke, and peripheral vascular disease, is genetically complex and the genes that confer cardiovascular risk remain largely unknown.… (more)

Subjects/Keywords: Medical sciences; Genetics; Molecular biology

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APA (6th Edition):

Kuo, C. (2011). Characterization ofAthsq1, an Atherosclerosis Modifier Locus on Mouse Chromosome 4:. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8CV4QXC

Chicago Manual of Style (16th Edition):

Kuo, Chao-Ling. “Characterization ofAthsq1, an Atherosclerosis Modifier Locus on Mouse Chromosome 4:.” 2011. Doctoral Dissertation, Columbia University. Accessed September 17, 2019. https://doi.org/10.7916/D8CV4QXC.

MLA Handbook (7th Edition):

Kuo, Chao-Ling. “Characterization ofAthsq1, an Atherosclerosis Modifier Locus on Mouse Chromosome 4:.” 2011. Web. 17 Sep 2019.

Vancouver:

Kuo C. Characterization ofAthsq1, an Atherosclerosis Modifier Locus on Mouse Chromosome 4:. [Internet] [Doctoral dissertation]. Columbia University; 2011. [cited 2019 Sep 17]. Available from: https://doi.org/10.7916/D8CV4QXC.

Council of Science Editors:

Kuo C. Characterization ofAthsq1, an Atherosclerosis Modifier Locus on Mouse Chromosome 4:. [Doctoral Dissertation]. Columbia University; 2011. Available from: https://doi.org/10.7916/D8CV4QXC

15. Hes, Frederik Jan. Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands.

Degree: 2000, University Utrecht

 Von Hippel-Lindau (VHL) disease is an autosomal, dominant inherited tumour syndrome. The disease is named after the German ophthalmologist Eugen von Hippel, who described retinal… (more)

Subjects/Keywords: Medical genetics

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APA (6th Edition):

Hes, F. J. (2000). Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/363 ; URN:NBN:NL:UI:10-1874-363 ; URN:NBN:NL:UI:10-1874-363 ; http://dspace.library.uu.nl/handle/1874/363

Chicago Manual of Style (16th Edition):

Hes, Frederik Jan. “Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands.” 2000. Doctoral Dissertation, University Utrecht. Accessed September 17, 2019. http://dspace.library.uu.nl/handle/1874/363 ; URN:NBN:NL:UI:10-1874-363 ; URN:NBN:NL:UI:10-1874-363 ; http://dspace.library.uu.nl/handle/1874/363.

MLA Handbook (7th Edition):

Hes, Frederik Jan. “Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands.” 2000. Web. 17 Sep 2019.

Vancouver:

Hes FJ. Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands. [Internet] [Doctoral dissertation]. University Utrecht; 2000. [cited 2019 Sep 17]. Available from: http://dspace.library.uu.nl/handle/1874/363 ; URN:NBN:NL:UI:10-1874-363 ; URN:NBN:NL:UI:10-1874-363 ; http://dspace.library.uu.nl/handle/1874/363.

Council of Science Editors:

Hes FJ. Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands. [Doctoral Dissertation]. University Utrecht; 2000. Available from: http://dspace.library.uu.nl/handle/1874/363 ; URN:NBN:NL:UI:10-1874-363 ; URN:NBN:NL:UI:10-1874-363 ; http://dspace.library.uu.nl/handle/1874/363

16. Hes, Frederik Jan. Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands.

Degree: 2000, University Utrecht

 Von Hippel-Lindau (VHL) disease is an autosomal, dominant inherited tumour syndrome. The disease is named after the German ophthalmologist Eugen von Hippel, who described retinal… (more)

Subjects/Keywords: Medical genetics

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

APA (6th Edition):

Hes, F. J. (2000). Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/363 ; URN:NBN:NL:UI:10-1874-363 ; URN:NBN:NL:UI:10-1874-363 ; http://dspace.library.uu.nl/handle/1874/363

Chicago Manual of Style (16th Edition):

Hes, Frederik Jan. “Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands.” 2000. Doctoral Dissertation, University Utrecht. Accessed September 17, 2019. http://dspace.library.uu.nl/handle/1874/363 ; URN:NBN:NL:UI:10-1874-363 ; URN:NBN:NL:UI:10-1874-363 ; http://dspace.library.uu.nl/handle/1874/363.

MLA Handbook (7th Edition):

Hes, Frederik Jan. “Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands.” 2000. Web. 17 Sep 2019.

Vancouver:

Hes FJ. Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands. [Internet] [Doctoral dissertation]. University Utrecht; 2000. [cited 2019 Sep 17]. Available from: http://dspace.library.uu.nl/handle/1874/363 ; URN:NBN:NL:UI:10-1874-363 ; URN:NBN:NL:UI:10-1874-363 ; http://dspace.library.uu.nl/handle/1874/363.

Council of Science Editors:

Hes FJ. Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands. [Doctoral Dissertation]. University Utrecht; 2000. Available from: http://dspace.library.uu.nl/handle/1874/363 ; URN:NBN:NL:UI:10-1874-363 ; URN:NBN:NL:UI:10-1874-363 ; http://dspace.library.uu.nl/handle/1874/363


University of Cape Town

17. Pretorius, Careni Elizabeth. A clinical and molecular investigation of two families with Simpson-Golabi-Behmel syndrome.

Degree: Image, Division of Human Genetics, 2014, University of Cape Town

Includes abstract (p. 30-32). Includes bibliographical references. Advisors/Committee Members: Fieggen, Karen (advisor), Beighton, Peter (advisor).

Subjects/Keywords: Medical Genetics

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

APA (6th Edition):

Pretorius, C. E. (2014). A clinical and molecular investigation of two families with Simpson-Golabi-Behmel syndrome. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/6006

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):

Pretorius, Careni Elizabeth. “A clinical and molecular investigation of two families with Simpson-Golabi-Behmel syndrome.” 2014. Thesis, University of Cape Town. Accessed September 17, 2019. http://hdl.handle.net/11427/6006.

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

MLA Handbook (7th Edition):

Pretorius, Careni Elizabeth. “A clinical and molecular investigation of two families with Simpson-Golabi-Behmel syndrome.” 2014. Web. 17 Sep 2019.

Vancouver:

Pretorius CE. A clinical and molecular investigation of two families with Simpson-Golabi-Behmel syndrome. [Internet] [Thesis]. University of Cape Town; 2014. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/11427/6006.

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

Council of Science Editors:

Pretorius CE. A clinical and molecular investigation of two families with Simpson-Golabi-Behmel syndrome. [Thesis]. University of Cape Town; 2014. Available from: http://hdl.handle.net/11427/6006

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


University of Oxford

18. Nudel, Ron. Molecular genetics of language impairment.

Degree: PhD, 2015, University of Oxford

 Developmental language impairments are neurodevelopmental disorders in which the acquisition of language, a task which children typically perform with ease, is hindered or fraught with… (more)

Subjects/Keywords: 616.85; Medical Sciences; Clinical genetics; Genetics (medical sciences); Neuroscience; Neurogenetics; Genetics; Communication Disorders; Neurosciences; Genetics,Behavioral; Genetics,Medical

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APA (6th Edition):

Nudel, R. (2015). Molecular genetics of language impairment. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:70249129-ef2e-4508-b8f6-50d6eae8e78b ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.640099

Chicago Manual of Style (16th Edition):

Nudel, Ron. “Molecular genetics of language impairment.” 2015. Doctoral Dissertation, University of Oxford. Accessed September 17, 2019. http://ora.ox.ac.uk/objects/uuid:70249129-ef2e-4508-b8f6-50d6eae8e78b ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.640099.

MLA Handbook (7th Edition):

Nudel, Ron. “Molecular genetics of language impairment.” 2015. Web. 17 Sep 2019.

Vancouver:

Nudel R. Molecular genetics of language impairment. [Internet] [Doctoral dissertation]. University of Oxford; 2015. [cited 2019 Sep 17]. Available from: http://ora.ox.ac.uk/objects/uuid:70249129-ef2e-4508-b8f6-50d6eae8e78b ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.640099.

Council of Science Editors:

Nudel R. Molecular genetics of language impairment. [Doctoral Dissertation]. University of Oxford; 2015. Available from: http://ora.ox.ac.uk/objects/uuid:70249129-ef2e-4508-b8f6-50d6eae8e78b ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.640099

19. Andersson, Emma. Characterization of mature T-cell leukemias by next-generation sequencing and drug sensitivity testing.

Degree: Institute of Clinical Medicine, Hematology Research Unit, Department of Clinical Chemistry and Hematology, University of Helsinki; Helsinki University Hospital Comprehensive Cancer Center, Department of Hematology, 2017, University of Helsinki

 Mature T-cell malignancies comprise a heterogeneous group of diseases with widely variable clinical courses, ranging from indolent, slowly progressing to rapidly progressing disease, leading to… (more)

Subjects/Keywords: medical genetics; medical genetics

…Nature Genetics 2011)117 and Grossmann et al. (Blood 2011)118 reported the… 

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APA (6th Edition):

Andersson, E. (2017). Characterization of mature T-cell leukemias by next-generation sequencing and drug sensitivity testing. (Doctoral Dissertation). University of Helsinki. Retrieved from http://hdl.handle.net/10138/172870

Chicago Manual of Style (16th Edition):

Andersson, Emma. “Characterization of mature T-cell leukemias by next-generation sequencing and drug sensitivity testing.” 2017. Doctoral Dissertation, University of Helsinki. Accessed September 17, 2019. http://hdl.handle.net/10138/172870.

MLA Handbook (7th Edition):

Andersson, Emma. “Characterization of mature T-cell leukemias by next-generation sequencing and drug sensitivity testing.” 2017. Web. 17 Sep 2019.

Vancouver:

Andersson E. Characterization of mature T-cell leukemias by next-generation sequencing and drug sensitivity testing. [Internet] [Doctoral dissertation]. University of Helsinki; 2017. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/10138/172870.

Council of Science Editors:

Andersson E. Characterization of mature T-cell leukemias by next-generation sequencing and drug sensitivity testing. [Doctoral Dissertation]. University of Helsinki; 2017. Available from: http://hdl.handle.net/10138/172870

20. Kanduri, Chakravarthi. Genomics approaches to study music perception and performance.

Degree: Haartman Institute, Faculty of Medicine, 2015, University of Helsinki

Music perception and performance form a useful tool for studying the normal functioning of the human brain. The abundance of neuroscientific literature has demonstrated that… (more)

Subjects/Keywords: Medical Genetics; Medical Genetics

genetics research has drastically advanced at a rapid pace post-HGP (Table 1). Table 1… …microarrays in medical research are from cancer studies, where microarrays have been successfully… …fields of genetics and genomics 6,113–115. Several studies have compared and described DNA… 

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APA (6th Edition):

Kanduri, C. (2015). Genomics approaches to study music perception and performance. (Doctoral Dissertation). University of Helsinki. Retrieved from http://hdl.handle.net/10138/155397

Chicago Manual of Style (16th Edition):

Kanduri, Chakravarthi. “Genomics approaches to study music perception and performance.” 2015. Doctoral Dissertation, University of Helsinki. Accessed September 17, 2019. http://hdl.handle.net/10138/155397.

MLA Handbook (7th Edition):

Kanduri, Chakravarthi. “Genomics approaches to study music perception and performance.” 2015. Web. 17 Sep 2019.

Vancouver:

Kanduri C. Genomics approaches to study music perception and performance. [Internet] [Doctoral dissertation]. University of Helsinki; 2015. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/10138/155397.

Council of Science Editors:

Kanduri C. Genomics approaches to study music perception and performance. [Doctoral Dissertation]. University of Helsinki; 2015. Available from: http://hdl.handle.net/10138/155397


Virginia Commonwealth University

21. Quinn, Bridget A. Novel Therapeutic Strategies for Pancreatic Cancer.

Degree: PhD, Human Genetics, 2014, Virginia Commonwealth University

  Pancreatic cancer is a devastating disease that leaves patients with a very poor prognosis and few therapeutic options. Many of the treatment options available… (more)

Subjects/Keywords: Medical Cell Biology; Medical Genetics; Neoplasms; Oncology; Translational Medical Research

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APA (6th Edition):

Quinn, B. A. (2014). Novel Therapeutic Strategies for Pancreatic Cancer. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/4671

Chicago Manual of Style (16th Edition):

Quinn, Bridget A. “Novel Therapeutic Strategies for Pancreatic Cancer.” 2014. Doctoral Dissertation, Virginia Commonwealth University. Accessed September 17, 2019. https://scholarscompass.vcu.edu/etd/4671.

MLA Handbook (7th Edition):

Quinn, Bridget A. “Novel Therapeutic Strategies for Pancreatic Cancer.” 2014. Web. 17 Sep 2019.

Vancouver:

Quinn BA. Novel Therapeutic Strategies for Pancreatic Cancer. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2014. [cited 2019 Sep 17]. Available from: https://scholarscompass.vcu.edu/etd/4671.

Council of Science Editors:

Quinn BA. Novel Therapeutic Strategies for Pancreatic Cancer. [Doctoral Dissertation]. Virginia Commonwealth University; 2014. Available from: https://scholarscompass.vcu.edu/etd/4671


Virginia Commonwealth University

22. Alsharief, Fahda Fawaz. Role of Translation Initiation in Regulation of Epithelial Junctions and Cell Motility.

Degree: MS, Molecular Biology and Genetics, 2017, Virginia Commonwealth University

  The integrity and barrier properties of intestinal epithelium are determined by specialized adhesive structures known as intercellular junctions; composed of adherens junctions (AJs), tight… (more)

Subjects/Keywords: Medical Biophysics; Medical Cell Biology; Medical Genetics; Physiological Processes

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APA (6th Edition):

Alsharief, F. F. (2017). Role of Translation Initiation in Regulation of Epithelial Junctions and Cell Motility. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/5018

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):

Alsharief, Fahda Fawaz. “Role of Translation Initiation in Regulation of Epithelial Junctions and Cell Motility.” 2017. Thesis, Virginia Commonwealth University. Accessed September 17, 2019. https://scholarscompass.vcu.edu/etd/5018.

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

MLA Handbook (7th Edition):

Alsharief, Fahda Fawaz. “Role of Translation Initiation in Regulation of Epithelial Junctions and Cell Motility.” 2017. Web. 17 Sep 2019.

Vancouver:

Alsharief FF. Role of Translation Initiation in Regulation of Epithelial Junctions and Cell Motility. [Internet] [Thesis]. Virginia Commonwealth University; 2017. [cited 2019 Sep 17]. Available from: https://scholarscompass.vcu.edu/etd/5018.

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

Council of Science Editors:

Alsharief FF. Role of Translation Initiation in Regulation of Epithelial Junctions and Cell Motility. [Thesis]. Virginia Commonwealth University; 2017. Available from: https://scholarscompass.vcu.edu/etd/5018

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


Western Kentucky University

23. Wright, Alice Ann. The Genomic Sequence and Annotation of Bacteriophage HK239.

Degree: Masters of Biology, Department of Biology, 2010, Western Kentucky University

 Bacteriophages are viruses that infect bacteria and they are the most numerous biological entities on Earth. Temperate phage can adopt two different lifestyles. In the… (more)

Subjects/Keywords: medical genetics; biotechnology; bacterial genetics; molecular virology; Biotechnology; Genetics; Genetics and Genomics

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APA (6th Edition):

Wright, A. A. (2010). The Genomic Sequence and Annotation of Bacteriophage HK239. (Masters Thesis). Western Kentucky University. Retrieved from https://digitalcommons.wku.edu/theses/208

Chicago Manual of Style (16th Edition):

Wright, Alice Ann. “The Genomic Sequence and Annotation of Bacteriophage HK239.” 2010. Masters Thesis, Western Kentucky University. Accessed September 17, 2019. https://digitalcommons.wku.edu/theses/208.

MLA Handbook (7th Edition):

Wright, Alice Ann. “The Genomic Sequence and Annotation of Bacteriophage HK239.” 2010. Web. 17 Sep 2019.

Vancouver:

Wright AA. The Genomic Sequence and Annotation of Bacteriophage HK239. [Internet] [Masters thesis]. Western Kentucky University; 2010. [cited 2019 Sep 17]. Available from: https://digitalcommons.wku.edu/theses/208.

Council of Science Editors:

Wright AA. The Genomic Sequence and Annotation of Bacteriophage HK239. [Masters Thesis]. Western Kentucky University; 2010. Available from: https://digitalcommons.wku.edu/theses/208


Texas Medical Center

24. Penney, Samantha. Evaluation of Knowledge Regarding Diagnostic Strategies for Genetic Diseases in Select Residents.

Degree: MS, 2012, Texas Medical Center

Genetics education for physicians has been a popular publication topic in the United States and in Europe for over 20 years. Decreasing numbers of… (more)

Subjects/Keywords: CMA; resident knowledge; genetics education; medical genetics; microarray; genetic testing; clinical genetics primary care; genetics; pediatrics; physician knowledge; medical education; Medical Education; Medical Genetics; Medicine and Health Sciences

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APA (6th Edition):

Penney, S. (2012). Evaluation of Knowledge Regarding Diagnostic Strategies for Genetic Diseases in Select Residents. (Masters Thesis). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/257

Chicago Manual of Style (16th Edition):

Penney, Samantha. “Evaluation of Knowledge Regarding Diagnostic Strategies for Genetic Diseases in Select Residents.” 2012. Masters Thesis, Texas Medical Center. Accessed September 17, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/257.

MLA Handbook (7th Edition):

Penney, Samantha. “Evaluation of Knowledge Regarding Diagnostic Strategies for Genetic Diseases in Select Residents.” 2012. Web. 17 Sep 2019.

Vancouver:

Penney S. Evaluation of Knowledge Regarding Diagnostic Strategies for Genetic Diseases in Select Residents. [Internet] [Masters thesis]. Texas Medical Center; 2012. [cited 2019 Sep 17]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/257.

Council of Science Editors:

Penney S. Evaluation of Knowledge Regarding Diagnostic Strategies for Genetic Diseases in Select Residents. [Masters Thesis]. Texas Medical Center; 2012. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/257


University of Oxford

25. Wong, Hei Sunny. Genetic susceptibility to common mycobacterial diseases.

Degree: PhD, 2010, University of Oxford

 Common mycobacterial diseases, including tuberculosis and leprosy, contribute to major mortality and morbidity worldwide. Despite evidence of an important role of host genetic factors in… (more)

Subjects/Keywords: 616.9; Medical Sciences; Clinical genetics; Infectious diseases; Biology (medical sciences); Genetics (medical sciences); Evolution (zoology); genetics; susceptibility; mycobacteria; tuberculosis; leprosy

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APA (6th Edition):

Wong, H. S. (2010). Genetic susceptibility to common mycobacterial diseases. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:cb4dd818-4693-4168-ad8a-cdeb59e2d5f3 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.526415

Chicago Manual of Style (16th Edition):

Wong, Hei Sunny. “Genetic susceptibility to common mycobacterial diseases.” 2010. Doctoral Dissertation, University of Oxford. Accessed September 17, 2019. http://ora.ox.ac.uk/objects/uuid:cb4dd818-4693-4168-ad8a-cdeb59e2d5f3 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.526415.

MLA Handbook (7th Edition):

Wong, Hei Sunny. “Genetic susceptibility to common mycobacterial diseases.” 2010. Web. 17 Sep 2019.

Vancouver:

Wong HS. Genetic susceptibility to common mycobacterial diseases. [Internet] [Doctoral dissertation]. University of Oxford; 2010. [cited 2019 Sep 17]. Available from: http://ora.ox.ac.uk/objects/uuid:cb4dd818-4693-4168-ad8a-cdeb59e2d5f3 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.526415.

Council of Science Editors:

Wong HS. Genetic susceptibility to common mycobacterial diseases. [Doctoral Dissertation]. University of Oxford; 2010. Available from: http://ora.ox.ac.uk/objects/uuid:cb4dd818-4693-4168-ad8a-cdeb59e2d5f3 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.526415


Universiteit Utrecht

26. Hes, Frederik Jan. Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands.

Degree: 2000, Universiteit Utrecht

 Von Hippel-Lindau (VHL) disease is an autosomal, dominant inherited tumour syndrome. The disease is named after the German ophthalmologist Eugen von Hippel, who described retinal… (more)

Subjects/Keywords: Geneeskunde; Medical genetics

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APA (6th Edition):

Hes, F. J. (2000). Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/363

Chicago Manual of Style (16th Edition):

Hes, Frederik Jan. “Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands.” 2000. Doctoral Dissertation, Universiteit Utrecht. Accessed September 17, 2019. http://dspace.library.uu.nl:8080/handle/1874/363.

MLA Handbook (7th Edition):

Hes, Frederik Jan. “Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands.” 2000. Web. 17 Sep 2019.

Vancouver:

Hes FJ. Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2000. [cited 2019 Sep 17]. Available from: http://dspace.library.uu.nl:8080/handle/1874/363.

Council of Science Editors:

Hes FJ. Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands. [Doctoral Dissertation]. Universiteit Utrecht; 2000. Available from: http://dspace.library.uu.nl:8080/handle/1874/363


UCLA

27. Sorensen, Page Lundy. Parent Reactions to Fragile X Premutation Diagnosis in the Newborn Period.

Degree: Anthropology, 2014, UCLA

 This paper explores fragile X newborn screening (FXNBS) from the perspective of parents whose newborns were diagnosed as FX premutation carriers as a result of… (more)

Subjects/Keywords: Genetics; Medical ethics; fragile X; Newborn Screening

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APA (6th Edition):

Sorensen, P. L. (2014). Parent Reactions to Fragile X Premutation Diagnosis in the Newborn Period. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/38n6g65b

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):

Sorensen, Page Lundy. “Parent Reactions to Fragile X Premutation Diagnosis in the Newborn Period.” 2014. Thesis, UCLA. Accessed September 17, 2019. http://www.escholarship.org/uc/item/38n6g65b.

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

MLA Handbook (7th Edition):

Sorensen, Page Lundy. “Parent Reactions to Fragile X Premutation Diagnosis in the Newborn Period.” 2014. Web. 17 Sep 2019.

Vancouver:

Sorensen PL. Parent Reactions to Fragile X Premutation Diagnosis in the Newborn Period. [Internet] [Thesis]. UCLA; 2014. [cited 2019 Sep 17]. Available from: http://www.escholarship.org/uc/item/38n6g65b.

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

Council of Science Editors:

Sorensen PL. Parent Reactions to Fragile X Premutation Diagnosis in the Newborn Period. [Thesis]. UCLA; 2014. Available from: http://www.escholarship.org/uc/item/38n6g65b

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


McGill University

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

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

Subjects/Keywords: Thalassemia.; Medical genetics.

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Heath, V Ann. “A screening program for the detection of beta thalassemia heterozygotes.” 1974. Masters Thesis, McGill University. Accessed September 17, 2019. http://digitool.library.mcgill.ca/thesisfile51896.pdf.

MLA Handbook (7th Edition):

Heath, V Ann. “A screening program for the detection of beta thalassemia heterozygotes.” 1974. Web. 17 Sep 2019.

Vancouver:

Heath VA. A screening program for the detection of beta thalassemia heterozygotes. [Internet] [Masters thesis]. McGill University; 1974. [cited 2019 Sep 17]. Available from: http://digitool.library.mcgill.ca/thesisfile51896.pdf.

Council of Science Editors:

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


University of Oxford

29. Davenport, Emma Elisabeth. Functional genomics of variation in response to infection : insights into severe sepsis and common variable immune deficiency disorders.

Degree: PhD, 2014, University of Oxford

 Functional genomics uses high throughput genome-wide technologies to investigate the functional consequences of genetic variants on gene expression and protein products. In the context of… (more)

Subjects/Keywords: 616.07; Genetics (medical sciences); Functional genomics; immunology

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APA (6th Edition):

Davenport, E. E. (2014). Functional genomics of variation in response to infection : insights into severe sepsis and common variable immune deficiency disorders. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:528edf20-f948-4a9c-aa23-1e295b11c8cc ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644672

Chicago Manual of Style (16th Edition):

Davenport, Emma Elisabeth. “Functional genomics of variation in response to infection : insights into severe sepsis and common variable immune deficiency disorders.” 2014. Doctoral Dissertation, University of Oxford. Accessed September 17, 2019. http://ora.ox.ac.uk/objects/uuid:528edf20-f948-4a9c-aa23-1e295b11c8cc ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644672.

MLA Handbook (7th Edition):

Davenport, Emma Elisabeth. “Functional genomics of variation in response to infection : insights into severe sepsis and common variable immune deficiency disorders.” 2014. Web. 17 Sep 2019.

Vancouver:

Davenport EE. Functional genomics of variation in response to infection : insights into severe sepsis and common variable immune deficiency disorders. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2019 Sep 17]. Available from: http://ora.ox.ac.uk/objects/uuid:528edf20-f948-4a9c-aa23-1e295b11c8cc ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644672.

Council of Science Editors:

Davenport EE. Functional genomics of variation in response to infection : insights into severe sepsis and common variable immune deficiency disorders. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:528edf20-f948-4a9c-aa23-1e295b11c8cc ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644672

30. Andrews, Verity A. Genetics and genomics in nursing : what are the characteristics of genetic nurse adopters and nurse opinion leaders in genetics and genomics?.

Degree: PhD, 2012, University of South Wales

 Background. Aspects of genetics/genomics are increasingly being incorporated into medicine. Nurses are crucial in helping transform healthcare through genomic nursing (Loud, 2010). However the integration… (more)

Subjects/Keywords: 610.73; Medical genetics; Genomes; Nursing; nursing education

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

APA (6th Edition):

Andrews, V. A. (2012). Genetics and genomics in nursing : what are the characteristics of genetic nurse adopters and nurse opinion leaders in genetics and genomics?. (Doctoral Dissertation). University of South Wales. Retrieved from https://pure.southwales.ac.uk/en/studentthesis/genetics-and-genomics-in-nursing(237c7d78-1001-4039-9c54-e694eae69dc9).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.589402

Chicago Manual of Style (16th Edition):

Andrews, Verity A. “Genetics and genomics in nursing : what are the characteristics of genetic nurse adopters and nurse opinion leaders in genetics and genomics?.” 2012. Doctoral Dissertation, University of South Wales. Accessed September 17, 2019. https://pure.southwales.ac.uk/en/studentthesis/genetics-and-genomics-in-nursing(237c7d78-1001-4039-9c54-e694eae69dc9).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.589402.

MLA Handbook (7th Edition):

Andrews, Verity A. “Genetics and genomics in nursing : what are the characteristics of genetic nurse adopters and nurse opinion leaders in genetics and genomics?.” 2012. Web. 17 Sep 2019.

Vancouver:

Andrews VA. Genetics and genomics in nursing : what are the characteristics of genetic nurse adopters and nurse opinion leaders in genetics and genomics?. [Internet] [Doctoral dissertation]. University of South Wales; 2012. [cited 2019 Sep 17]. Available from: https://pure.southwales.ac.uk/en/studentthesis/genetics-and-genomics-in-nursing(237c7d78-1001-4039-9c54-e694eae69dc9).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.589402.

Council of Science Editors:

Andrews VA. Genetics and genomics in nursing : what are the characteristics of genetic nurse adopters and nurse opinion leaders in genetics and genomics?. [Doctoral Dissertation]. University of South Wales; 2012. Available from: https://pure.southwales.ac.uk/en/studentthesis/genetics-and-genomics-in-nursing(237c7d78-1001-4039-9c54-e694eae69dc9).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.589402

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