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You searched for subject:(Medical Genetics). Showing records 1 – 30 of 705 total matches.

[1] [2] [3] [4] [5] … [24]

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

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 October 22, 2020. 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. 22 Oct 2020.

Vancouver:

Vlachopoulou E. HLA-DRB1: Haplotype Diversity, Imputation and Association with Acute Coronary Syndrome. [Internet] [Doctoral dissertation]. University of Helsinki; 2015. [cited 2020 Oct 22]. 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


Virginia Commonwealth University

2. 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://doi.org/10.25772/3TN5-5R02 ; 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 October 22, 2020. https://doi.org/10.25772/3TN5-5R02 ; 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. 22 Oct 2020.

Vancouver:

Peterson KN. Investigating the Role of Bptf in Immunoediting in Breast Cancer and Melanoma. [Internet] [Thesis]. Virginia Commonwealth University; 2015. [cited 2020 Oct 22]. Available from: https://doi.org/10.25772/3TN5-5R02 ; 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://doi.org/10.25772/3TN5-5R02 ; 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 Cape Town

3. 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 October 22, 2020. 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. 22 Oct 2020.

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 2020 Oct 22]. 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

4. Kitaba, Negusse Tadesse. Development of models for the action of novel anti-apoptotic proteins using gene regulation, pathway analysis and protein structure prediction.

Degree: PhD, 2015, University of South Wales

 Cancer refers to a large and complex group of diseases that can be caused by multiple genetic and environmental factors. Many cancers are associated with… (more)

Subjects/Keywords: Medical genetics

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APA (6th Edition):

Kitaba, N. T. (2015). Development of models for the action of novel anti-apoptotic proteins using gene regulation, pathway analysis and protein structure prediction. (Doctoral Dissertation). University of South Wales. Retrieved from https://pure.southwales.ac.uk/en/studentthesis/development-of-models-for-the-action-of-novel-antiapoptotic-proteins-using-gene-regulation-pathway-analysis-and-protein-structure-prediction(8b15b6f6-0f36-49e6-85f9-64ebed610c1f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.795290

Chicago Manual of Style (16th Edition):

Kitaba, Negusse Tadesse. “Development of models for the action of novel anti-apoptotic proteins using gene regulation, pathway analysis and protein structure prediction.” 2015. Doctoral Dissertation, University of South Wales. Accessed October 22, 2020. https://pure.southwales.ac.uk/en/studentthesis/development-of-models-for-the-action-of-novel-antiapoptotic-proteins-using-gene-regulation-pathway-analysis-and-protein-structure-prediction(8b15b6f6-0f36-49e6-85f9-64ebed610c1f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.795290.

MLA Handbook (7th Edition):

Kitaba, Negusse Tadesse. “Development of models for the action of novel anti-apoptotic proteins using gene regulation, pathway analysis and protein structure prediction.” 2015. Web. 22 Oct 2020.

Vancouver:

Kitaba NT. Development of models for the action of novel anti-apoptotic proteins using gene regulation, pathway analysis and protein structure prediction. [Internet] [Doctoral dissertation]. University of South Wales; 2015. [cited 2020 Oct 22]. Available from: https://pure.southwales.ac.uk/en/studentthesis/development-of-models-for-the-action-of-novel-antiapoptotic-proteins-using-gene-regulation-pathway-analysis-and-protein-structure-prediction(8b15b6f6-0f36-49e6-85f9-64ebed610c1f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.795290.

Council of Science Editors:

Kitaba NT. Development of models for the action of novel anti-apoptotic proteins using gene regulation, pathway analysis and protein structure prediction. [Doctoral Dissertation]. University of South Wales; 2015. Available from: https://pure.southwales.ac.uk/en/studentthesis/development-of-models-for-the-action-of-novel-antiapoptotic-proteins-using-gene-regulation-pathway-analysis-and-protein-structure-prediction(8b15b6f6-0f36-49e6-85f9-64ebed610c1f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.795290


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 October 22, 2020. 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. 22 Oct 2020.

Vancouver:

Beatty L. Adiponectin Receptor 1 and Liver Kinase B1 are Downregulated in Renal Cell Carcinoma. [Internet] [Masters thesis]. McMaster University; 2011. [cited 2020 Oct 22]. 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 October 22, 2020. 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. 22 Oct 2020.

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 2020 Oct 22]. 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 October 22, 2020. 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. 22 Oct 2020.

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 2020 Oct 22]. 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


Columbia University

8. Olguin, Arturo. A Review of Genetic Transfer Therapy Trials from a Regulatory Perspective for the Scientific Understanding.

Degree: 2013, Columbia University

 The present work reviews the safety and efficacy concerns of the Recombinant DNA Advisory Committee (RAC) regarding Gene Transfer Therapy (GTT) clinical trials. The RAC,… (more)

Subjects/Keywords: Medical ethics; Genetics

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APA (6th Edition):

Olguin, A. (2013). A Review of Genetic Transfer Therapy Trials from a Regulatory Perspective for the Scientific Understanding. (Masters Thesis). Columbia University. Retrieved from https://doi.org/10.7916/D8PN9CVZ

Chicago Manual of Style (16th Edition):

Olguin, Arturo. “A Review of Genetic Transfer Therapy Trials from a Regulatory Perspective for the Scientific Understanding.” 2013. Masters Thesis, Columbia University. Accessed October 22, 2020. https://doi.org/10.7916/D8PN9CVZ.

MLA Handbook (7th Edition):

Olguin, Arturo. “A Review of Genetic Transfer Therapy Trials from a Regulatory Perspective for the Scientific Understanding.” 2013. Web. 22 Oct 2020.

Vancouver:

Olguin A. A Review of Genetic Transfer Therapy Trials from a Regulatory Perspective for the Scientific Understanding. [Internet] [Masters thesis]. Columbia University; 2013. [cited 2020 Oct 22]. Available from: https://doi.org/10.7916/D8PN9CVZ.

Council of Science Editors:

Olguin A. A Review of Genetic Transfer Therapy Trials from a Regulatory Perspective for the Scientific Understanding. [Masters Thesis]. Columbia University; 2013. Available from: https://doi.org/10.7916/D8PN9CVZ


Columbia University

9. Brandt, Margot. Characterizing human regulatory genetic variation using CRISPR/Cas9 genome editing.

Degree: 2020, Columbia University

 Rare gene-disrupting variants and common regulatory variants play key roles in rare and common disease, respectively. These variants are of great interest for investigation into… (more)

Subjects/Keywords: Genetics; Human genetics – Variation; CRISPR (Genetics); Medical genetics; Gene editing

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APA (6th Edition):

Brandt, M. (2020). Characterizing human regulatory genetic variation using CRISPR/Cas9 genome editing. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/d8-h4zz-2953

Chicago Manual of Style (16th Edition):

Brandt, Margot. “Characterizing human regulatory genetic variation using CRISPR/Cas9 genome editing.” 2020. Doctoral Dissertation, Columbia University. Accessed October 22, 2020. https://doi.org/10.7916/d8-h4zz-2953.

MLA Handbook (7th Edition):

Brandt, Margot. “Characterizing human regulatory genetic variation using CRISPR/Cas9 genome editing.” 2020. Web. 22 Oct 2020.

Vancouver:

Brandt M. Characterizing human regulatory genetic variation using CRISPR/Cas9 genome editing. [Internet] [Doctoral dissertation]. Columbia University; 2020. [cited 2020 Oct 22]. Available from: https://doi.org/10.7916/d8-h4zz-2953.

Council of Science Editors:

Brandt M. Characterizing human regulatory genetic variation using CRISPR/Cas9 genome editing. [Doctoral Dissertation]. Columbia University; 2020. Available from: https://doi.org/10.7916/d8-h4zz-2953


University of Oxford

10. 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 October 22, 2020. 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. 22 Oct 2020.

Vancouver:

Shipman L. The functional consequences of autoimmune variants in the tyrosine kinase 2 gene region. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2020 Oct 22]. 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

11. 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 October 22, 2020. 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. 22 Oct 2020.

Vancouver:

Yen H. Development of the zebrafish as a model for Bardet-Biedl syndrome. [Internet] [Doctoral dissertation]. University of Iowa; 2007. [cited 2020 Oct 22]. 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 Oxford

12. 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 ; https://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 October 22, 2020. http://ora.ox.ac.uk/objects/uuid:70249129-ef2e-4508-b8f6-50d6eae8e78b ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.640099.

MLA Handbook (7th Edition):

Nudel, Ron. “Molecular genetics of language impairment.” 2015. Web. 22 Oct 2020.

Vancouver:

Nudel R. Molecular genetics of language impairment. [Internet] [Doctoral dissertation]. University of Oxford; 2015. [cited 2020 Oct 22]. Available from: http://ora.ox.ac.uk/objects/uuid:70249129-ef2e-4508-b8f6-50d6eae8e78b ; https://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 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.640099


University of Lund

13. Ågerstam, Helena. Molecular and functional studies of ABL1 and FGFR1 fusion oncogenes in myeloproliferative neoplasms.

Degree: 2010, University of Lund

 The tyrosine kinase encoding genes ABL1 and FGFR1 are involved in fusion genes underlying the myeloproliferative neoplasms chronic myeloid leukemia (CML) and the 8p11-myeloproliferative syndrome… (more)

Subjects/Keywords: Medical Genetics

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APA (6th Edition):

Ågerstam, H. (2010). Molecular and functional studies of ABL1 and FGFR1 fusion oncogenes in myeloproliferative neoplasms. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/1692678 ; https://portal.research.lu.se/ws/files/4283052/1692679.pdf

Chicago Manual of Style (16th Edition):

Ågerstam, Helena. “Molecular and functional studies of ABL1 and FGFR1 fusion oncogenes in myeloproliferative neoplasms.” 2010. Doctoral Dissertation, University of Lund. Accessed October 22, 2020. https://lup.lub.lu.se/record/1692678 ; https://portal.research.lu.se/ws/files/4283052/1692679.pdf.

MLA Handbook (7th Edition):

Ågerstam, Helena. “Molecular and functional studies of ABL1 and FGFR1 fusion oncogenes in myeloproliferative neoplasms.” 2010. Web. 22 Oct 2020.

Vancouver:

Ågerstam H. Molecular and functional studies of ABL1 and FGFR1 fusion oncogenes in myeloproliferative neoplasms. [Internet] [Doctoral dissertation]. University of Lund; 2010. [cited 2020 Oct 22]. Available from: https://lup.lub.lu.se/record/1692678 ; https://portal.research.lu.se/ws/files/4283052/1692679.pdf.

Council of Science Editors:

Ågerstam H. Molecular and functional studies of ABL1 and FGFR1 fusion oncogenes in myeloproliferative neoplasms. [Doctoral Dissertation]. University of Lund; 2010. Available from: https://lup.lub.lu.se/record/1692678 ; https://portal.research.lu.se/ws/files/4283052/1692679.pdf


University of Lund

14. Möller, Emely. EWSR1 and FUS fusion genes in tumorigenesis.

Degree: 2010, University of Lund

 The present thesis concerns the involvement of EWSR1 and FUS fusion genes, and the chimeric proteins they encode, in tumorigenesis. In Article I, the EWSR1… (more)

Subjects/Keywords: Medical Genetics

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APA (6th Edition):

Möller, E. (2010). EWSR1 and FUS fusion genes in tumorigenesis. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/1599164 ; https://portal.research.lu.se/ws/files/4032128/1599189.pdf

Chicago Manual of Style (16th Edition):

Möller, Emely. “EWSR1 and FUS fusion genes in tumorigenesis.” 2010. Doctoral Dissertation, University of Lund. Accessed October 22, 2020. https://lup.lub.lu.se/record/1599164 ; https://portal.research.lu.se/ws/files/4032128/1599189.pdf.

MLA Handbook (7th Edition):

Möller, Emely. “EWSR1 and FUS fusion genes in tumorigenesis.” 2010. Web. 22 Oct 2020.

Vancouver:

Möller E. EWSR1 and FUS fusion genes in tumorigenesis. [Internet] [Doctoral dissertation]. University of Lund; 2010. [cited 2020 Oct 22]. Available from: https://lup.lub.lu.se/record/1599164 ; https://portal.research.lu.se/ws/files/4032128/1599189.pdf.

Council of Science Editors:

Möller E. EWSR1 and FUS fusion genes in tumorigenesis. [Doctoral Dissertation]. University of Lund; 2010. Available from: https://lup.lub.lu.se/record/1599164 ; https://portal.research.lu.se/ws/files/4032128/1599189.pdf


University of Cape Town

15. 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 (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 October 22, 2020. 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. 22 Oct 2020.

Vancouver:

Pretorius CE. A clinical and molecular investigation of two families with Simpson-Golabi-Behmel syndrome. [Internet] [Thesis]. University of Cape Town; 2014. [cited 2020 Oct 22]. 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


Columbia University

16. 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 October 22, 2020. 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. 22 Oct 2020.

Vancouver:

Kuo C. Characterization ofAthsq1, an Atherosclerosis Modifier Locus on Mouse Chromosome 4:. [Internet] [Doctoral dissertation]. Columbia University; 2011. [cited 2020 Oct 22]. 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


University of Manitoba

17. Bungsy, Manisha. Determining the impact diminished RBX1 expression has on chromosome stability in cancer.

Degree: Biochemistry and Medical Genetics, 2019, University of Manitoba

 Chromosome instability (CIN) is an aberrant phenotype observed in nearly all cancer types including colorectal cancer and potentially, high-grade serous ovarian cancer (HGSOC). CIN is… (more)

Subjects/Keywords: Biochemistry; Medical Genetics; Ovarian Cancer

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APA (6th Edition):

Bungsy, M. (2019). Determining the impact diminished RBX1 expression has on chromosome stability in cancer. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/34482

Chicago Manual of Style (16th Edition):

Bungsy, Manisha. “Determining the impact diminished RBX1 expression has on chromosome stability in cancer.” 2019. Masters Thesis, University of Manitoba. Accessed October 22, 2020. http://hdl.handle.net/1993/34482.

MLA Handbook (7th Edition):

Bungsy, Manisha. “Determining the impact diminished RBX1 expression has on chromosome stability in cancer.” 2019. Web. 22 Oct 2020.

Vancouver:

Bungsy M. Determining the impact diminished RBX1 expression has on chromosome stability in cancer. [Internet] [Masters thesis]. University of Manitoba; 2019. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/1993/34482.

Council of Science Editors:

Bungsy M. Determining the impact diminished RBX1 expression has on chromosome stability in cancer. [Masters Thesis]. University of Manitoba; 2019. Available from: http://hdl.handle.net/1993/34482

18. 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 https://dspace.library.uu.nl/handle/1874/363 ; URN:NBN:NL:UI:10-1874-363 ; URN:NBN:NL:UI:10-1874-363 ; https://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 October 22, 2020. https://dspace.library.uu.nl/handle/1874/363 ; URN:NBN:NL:UI:10-1874-363 ; URN:NBN:NL:UI:10-1874-363 ; https://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. 22 Oct 2020.

Vancouver:

Hes FJ. Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands. [Internet] [Doctoral dissertation]. University Utrecht; 2000. [cited 2020 Oct 22]. Available from: https://dspace.library.uu.nl/handle/1874/363 ; URN:NBN:NL:UI:10-1874-363 ; URN:NBN:NL:UI:10-1874-363 ; https://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: https://dspace.library.uu.nl/handle/1874/363 ; URN:NBN:NL:UI:10-1874-363 ; URN:NBN:NL:UI:10-1874-363 ; https://dspace.library.uu.nl/handle/1874/363

19. 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 https://dspace.library.uu.nl/handle/1874/363 ; URN:NBN:NL:UI:10-1874-363 ; URN:NBN:NL:UI:10-1874-363 ; https://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 October 22, 2020. https://dspace.library.uu.nl/handle/1874/363 ; URN:NBN:NL:UI:10-1874-363 ; URN:NBN:NL:UI:10-1874-363 ; https://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. 22 Oct 2020.

Vancouver:

Hes FJ. Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands. [Internet] [Doctoral dissertation]. University Utrecht; 2000. [cited 2020 Oct 22]. Available from: https://dspace.library.uu.nl/handle/1874/363 ; URN:NBN:NL:UI:10-1874-363 ; URN:NBN:NL:UI:10-1874-363 ; https://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: https://dspace.library.uu.nl/handle/1874/363 ; URN:NBN:NL:UI:10-1874-363 ; URN:NBN:NL:UI:10-1874-363 ; https://dspace.library.uu.nl/handle/1874/363

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 October 22, 2020. http://hdl.handle.net/10138/155397.

MLA Handbook (7th Edition):

Kanduri, Chakravarthi. “Genomics approaches to study music perception and performance.” 2015. Web. 22 Oct 2020.

Vancouver:

Kanduri C. Genomics approaches to study music perception and performance. [Internet] [Doctoral dissertation]. University of Helsinki; 2015. [cited 2020 Oct 22]. 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

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

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 October 22, 2020. 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. 22 Oct 2020.

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 2020 Oct 22]. 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


Virginia Commonwealth University

22. 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://doi.org/10.25772/T39H-KJ31 ; 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 October 22, 2020. https://doi.org/10.25772/T39H-KJ31 ; https://scholarscompass.vcu.edu/etd/4671.

MLA Handbook (7th Edition):

Quinn, Bridget A. “Novel Therapeutic Strategies for Pancreatic Cancer.” 2014. Web. 22 Oct 2020.

Vancouver:

Quinn BA. Novel Therapeutic Strategies for Pancreatic Cancer. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2014. [cited 2020 Oct 22]. Available from: https://doi.org/10.25772/T39H-KJ31 ; 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://doi.org/10.25772/T39H-KJ31 ; https://scholarscompass.vcu.edu/etd/4671


Virginia Commonwealth University

23. 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://doi.org/10.25772/2VEH-V660 ; 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 October 22, 2020. https://doi.org/10.25772/2VEH-V660 ; 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. 22 Oct 2020.

Vancouver:

Alsharief FF. Role of Translation Initiation in Regulation of Epithelial Junctions and Cell Motility. [Internet] [Thesis]. Virginia Commonwealth University; 2017. [cited 2020 Oct 22]. Available from: https://doi.org/10.25772/2VEH-V660 ; 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://doi.org/10.25772/2VEH-V660 ; 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


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. (Thesis). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/257

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):

Penney, Samantha. “Evaluation of Knowledge Regarding Diagnostic Strategies for Genetic Diseases in Select Residents.” 2012. Thesis, Texas Medical Center. Accessed October 22, 2020. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/257.

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

MLA Handbook (7th Edition):

Penney, Samantha. “Evaluation of Knowledge Regarding Diagnostic Strategies for Genetic Diseases in Select Residents.” 2012. Web. 22 Oct 2020.

Vancouver:

Penney S. Evaluation of Knowledge Regarding Diagnostic Strategies for Genetic Diseases in Select Residents. [Internet] [Thesis]. Texas Medical Center; 2012. [cited 2020 Oct 22]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/257.

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

Council of Science Editors:

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

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


Universiteit Utrecht

25. 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 October 22, 2020. 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. 22 Oct 2020.

Vancouver:

Hes FJ. Von Hippel-Lindau disease: clinical and genetic investigations in the Netherlands. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2000. [cited 2020 Oct 22]. 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

26. 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 October 22, 2020. 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. 22 Oct 2020.

Vancouver:

Sorensen PL. Parent Reactions to Fragile X Premutation Diagnosis in the Newborn Period. [Internet] [Thesis]. UCLA; 2014. [cited 2020 Oct 22]. 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


Columbia University

27. [No author]. Genetic and Environmental Determinants of Alopecia Areata.

Degree: 2020, Columbia University

 Alopecia Areata (AA) is a highly prevalent autoimmune disease in the US with a lifetime risk of 2.1%. In AA, autoimmunity develops against the hair… (more)

Subjects/Keywords: Biology; Alopecia areata; Nutrition; Medical genetics – Research

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APA (6th Edition):

author], [. (2020). Genetic and Environmental Determinants of Alopecia Areata. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/d8-7wzy-zr95

Chicago Manual of Style (16th Edition):

author], [No. “Genetic and Environmental Determinants of Alopecia Areata.” 2020. Doctoral Dissertation, Columbia University. Accessed October 22, 2020. https://doi.org/10.7916/d8-7wzy-zr95.

MLA Handbook (7th Edition):

author], [No. “Genetic and Environmental Determinants of Alopecia Areata.” 2020. Web. 22 Oct 2020.

Vancouver:

author] [. Genetic and Environmental Determinants of Alopecia Areata. [Internet] [Doctoral dissertation]. Columbia University; 2020. [cited 2020 Oct 22]. Available from: https://doi.org/10.7916/d8-7wzy-zr95.

Council of Science Editors:

author] [. Genetic and Environmental Determinants of Alopecia Areata. [Doctoral Dissertation]. Columbia University; 2020. Available from: https://doi.org/10.7916/d8-7wzy-zr95


University of Lund

28. Lundberg, Gisela. Chromosome dynamics and genomic instablity in neuroblastoma. Three genomic pillars: MYCN amplification, numerical and structural changes.

Degree: 2012, University of Lund

 In this thesis, the main focus has been on the childhood cancer neuroblastoma, one of the most common and lethal childhood tumours. Neuroblastoma has througout… (more)

Subjects/Keywords: Medical Genetics; Neuroblastoma; MYCN; telomeres; chromosomal instability

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APA (6th Edition):

Lundberg, G. (2012). Chromosome dynamics and genomic instablity in neuroblastoma. Three genomic pillars: MYCN amplification, numerical and structural changes. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/3158484 ; https://portal.research.lu.se/ws/files/4225435/3158578.pdf

Chicago Manual of Style (16th Edition):

Lundberg, Gisela. “Chromosome dynamics and genomic instablity in neuroblastoma. Three genomic pillars: MYCN amplification, numerical and structural changes.” 2012. Doctoral Dissertation, University of Lund. Accessed October 22, 2020. https://lup.lub.lu.se/record/3158484 ; https://portal.research.lu.se/ws/files/4225435/3158578.pdf.

MLA Handbook (7th Edition):

Lundberg, Gisela. “Chromosome dynamics and genomic instablity in neuroblastoma. Three genomic pillars: MYCN amplification, numerical and structural changes.” 2012. Web. 22 Oct 2020.

Vancouver:

Lundberg G. Chromosome dynamics and genomic instablity in neuroblastoma. Three genomic pillars: MYCN amplification, numerical and structural changes. [Internet] [Doctoral dissertation]. University of Lund; 2012. [cited 2020 Oct 22]. Available from: https://lup.lub.lu.se/record/3158484 ; https://portal.research.lu.se/ws/files/4225435/3158578.pdf.

Council of Science Editors:

Lundberg G. Chromosome dynamics and genomic instablity in neuroblastoma. Three genomic pillars: MYCN amplification, numerical and structural changes. [Doctoral Dissertation]. University of Lund; 2012. Available from: https://lup.lub.lu.se/record/3158484 ; https://portal.research.lu.se/ws/files/4225435/3158578.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 · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

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 October 22, 2020. 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. 22 Oct 2020.

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 2020 Oct 22]. 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 October 22, 2020. 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. 22 Oct 2020.

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 2020 Oct 22]. 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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