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You searched for subject:(Genetic counselling). Showing records 1 – 30 of 37 total matches.

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University of Cape Town

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

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

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

Subjects/Keywords: Genetic Counselling

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

APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Al-Kharusi, Khalsa. “The experiences of couples undergoing Preimplantation Genetic Diagnosis (PGD) at the Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital (SQUH) in Oman.” 2016. Thesis, University of Cape Town. Accessed December 05, 2019. http://hdl.handle.net/11427/23776.

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

MLA Handbook (7th Edition):

Al-Kharusi, Khalsa. “The experiences of couples undergoing Preimplantation Genetic Diagnosis (PGD) at the Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital (SQUH) in Oman.” 2016. Web. 05 Dec 2019.

Vancouver:

Al-Kharusi K. The experiences of couples undergoing Preimplantation Genetic Diagnosis (PGD) at the Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital (SQUH) in Oman. [Internet] [Thesis]. University of Cape Town; 2016. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/11427/23776.

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

Council of Science Editors:

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

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


University of Cape Town

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

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

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

Subjects/Keywords: Genetic Counselling

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Ingram, Clair. “Perceptions of health-related quality of life among adults living with sickle cell disease in Cape Town, South Africa.” 2018. Thesis, University of Cape Town. Accessed December 05, 2019. http://hdl.handle.net/11427/27841.

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

MLA Handbook (7th Edition):

Ingram, Clair. “Perceptions of health-related quality of life among adults living with sickle cell disease in Cape Town, South Africa.” 2018. Web. 05 Dec 2019.

Vancouver:

Ingram C. Perceptions of health-related quality of life among adults living with sickle cell disease in Cape Town, South Africa. [Internet] [Thesis]. University of Cape Town; 2018. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/11427/27841.

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

Council of Science Editors:

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

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


University of Cape Town

3. Goliath, Rene. Exploration of the impact of genetic counselling and patient support group involvement on retinal degenerative disorders (RDD) patients: a qualitative study.

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

 This study explored the experiences of individuals within the clinical genetic service in South Africa, with inherited retinal disease. Methods: This qualitative research was based… (more)

Subjects/Keywords: Genetic Counselling

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APA (6th Edition):

Goliath, R. (2018). Exploration of the impact of genetic counselling and patient support group involvement on retinal degenerative disorders (RDD) patients: a qualitative study. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/27838

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):

Goliath, Rene. “Exploration of the impact of genetic counselling and patient support group involvement on retinal degenerative disorders (RDD) patients: a qualitative study.” 2018. Thesis, University of Cape Town. Accessed December 05, 2019. http://hdl.handle.net/11427/27838.

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

MLA Handbook (7th Edition):

Goliath, Rene. “Exploration of the impact of genetic counselling and patient support group involvement on retinal degenerative disorders (RDD) patients: a qualitative study.” 2018. Web. 05 Dec 2019.

Vancouver:

Goliath R. Exploration of the impact of genetic counselling and patient support group involvement on retinal degenerative disorders (RDD) patients: a qualitative study. [Internet] [Thesis]. University of Cape Town; 2018. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/11427/27838.

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

Council of Science Editors:

Goliath R. Exploration of the impact of genetic counselling and patient support group involvement on retinal degenerative disorders (RDD) patients: a qualitative study. [Thesis]. University of Cape Town; 2018. Available from: http://hdl.handle.net/11427/27838

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


University of Cape Town

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

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

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

Subjects/Keywords: Genetic Counselling

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Shaw, Tarryn. “Women's experiences of receiving a child's fetal alcohol spectrum disorder diagnosis: a Western Cape study.” 2015. Thesis, University of Cape Town. Accessed December 05, 2019. http://hdl.handle.net/11427/16922.

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

MLA Handbook (7th Edition):

Shaw, Tarryn. “Women's experiences of receiving a child's fetal alcohol spectrum disorder diagnosis: a Western Cape study.” 2015. Web. 05 Dec 2019.

Vancouver:

Shaw T. Women's experiences of receiving a child's fetal alcohol spectrum disorder diagnosis: a Western Cape study. [Internet] [Thesis]. University of Cape Town; 2015. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/11427/16922.

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

Council of Science Editors:

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

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


University of Cape Town

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

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

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

Subjects/Keywords: Genetic Counselling

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Verkijk, Nakita. “An investigation into the reasons for non-uptake of carrier testing in a family affected by alpha thalassaemia X-linked mental retardation (ATR-X) syndrome.” 2011. Thesis, University of Cape Town. Accessed December 05, 2019. http://hdl.handle.net/11427/11481.

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

MLA Handbook (7th Edition):

Verkijk, Nakita. “An investigation into the reasons for non-uptake of carrier testing in a family affected by alpha thalassaemia X-linked mental retardation (ATR-X) syndrome.” 2011. Web. 05 Dec 2019.

Vancouver:

Verkijk N. An investigation into the reasons for non-uptake of carrier testing in a family affected by alpha thalassaemia X-linked mental retardation (ATR-X) syndrome. [Internet] [Thesis]. University of Cape Town; 2011. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/11427/11481.

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

Council of Science Editors:

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

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


University of Cape Town

6. Araujo, Monica Rodrigues. Perspectives and Experiences of Individuals Undergoing Predictive Testing for Hereditary Breast and Ovarian Cancer (HBOC) Syndrome in the Western Cape, South Africa.

Degree: MSc, Pathology, 2018, University of Cape Town

 Breast cancer is the most common malignancy affecting females globally. Hereditary breast and ovarian cancer (HBOC) syndrome is caused by pathogenic variants in BRCA1 and… (more)

Subjects/Keywords: Genetic Counselling

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APA (6th Edition):

Araujo, M. R. (2018). Perspectives and Experiences of Individuals Undergoing Predictive Testing for Hereditary Breast and Ovarian Cancer (HBOC) Syndrome in the Western Cape, South Africa. (Masters Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/30057

Chicago Manual of Style (16th Edition):

Araujo, Monica Rodrigues. “Perspectives and Experiences of Individuals Undergoing Predictive Testing for Hereditary Breast and Ovarian Cancer (HBOC) Syndrome in the Western Cape, South Africa.” 2018. Masters Thesis, University of Cape Town. Accessed December 05, 2019. http://hdl.handle.net/11427/30057.

MLA Handbook (7th Edition):

Araujo, Monica Rodrigues. “Perspectives and Experiences of Individuals Undergoing Predictive Testing for Hereditary Breast and Ovarian Cancer (HBOC) Syndrome in the Western Cape, South Africa.” 2018. Web. 05 Dec 2019.

Vancouver:

Araujo MR. Perspectives and Experiences of Individuals Undergoing Predictive Testing for Hereditary Breast and Ovarian Cancer (HBOC) Syndrome in the Western Cape, South Africa. [Internet] [Masters thesis]. University of Cape Town; 2018. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/11427/30057.

Council of Science Editors:

Araujo MR. Perspectives and Experiences of Individuals Undergoing Predictive Testing for Hereditary Breast and Ovarian Cancer (HBOC) Syndrome in the Western Cape, South Africa. [Masters Thesis]. University of Cape Town; 2018. Available from: http://hdl.handle.net/11427/30057


University of Cape Town

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

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

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

Subjects/Keywords: Genetic Counselling

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

APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Malope, Malebo Felicia. “Exploring the decision making process of women offered termination of pregnancy for serious congenital abnormality.” 2018. Thesis, University of Cape Town. Accessed December 05, 2019. http://hdl.handle.net/11427/27900.

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

MLA Handbook (7th Edition):

Malope, Malebo Felicia. “Exploring the decision making process of women offered termination of pregnancy for serious congenital abnormality.” 2018. Web. 05 Dec 2019.

Vancouver:

Malope MF. Exploring the decision making process of women offered termination of pregnancy for serious congenital abnormality. [Internet] [Thesis]. University of Cape Town; 2018. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/11427/27900.

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

Council of Science Editors:

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

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


University of Cape Town

8. Popel, Kalinka. Young adults' perceptions of the implications of their hereditary, visual impairment: A Cape Town based study.

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

 In South Africa, approximately 600 000 individuals are visually impaired. Approximately onethird of genetic disorders and syndromes involves the eye, including conditions such as congenital… (more)

Subjects/Keywords: Genetic Counselling; Visual Impairment

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

APA (6th Edition):

Popel, K. (2017). Young adults' perceptions of the implications of their hereditary, visual impairment: A Cape Town based study. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/28181

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):

Popel, Kalinka. “Young adults' perceptions of the implications of their hereditary, visual impairment: A Cape Town based study.” 2017. Thesis, University of Cape Town. Accessed December 05, 2019. http://hdl.handle.net/11427/28181.

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

MLA Handbook (7th Edition):

Popel, Kalinka. “Young adults' perceptions of the implications of their hereditary, visual impairment: A Cape Town based study.” 2017. Web. 05 Dec 2019.

Vancouver:

Popel K. Young adults' perceptions of the implications of their hereditary, visual impairment: A Cape Town based study. [Internet] [Thesis]. University of Cape Town; 2017. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/11427/28181.

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

Council of Science Editors:

Popel K. Young adults' perceptions of the implications of their hereditary, visual impairment: A Cape Town based study. [Thesis]. University of Cape Town; 2017. Available from: http://hdl.handle.net/11427/28181

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


University of New South Wales

9. Zilliacus, Elvira Madeleine. Evaluating telehealth cancer genetic counselling: impact on genetic counselling outcomes, patient satisfaction and acceptability.

Degree: Psychiatry, 2010, University of New South Wales

 Telegenetics is increasingly being used to deliver familial cancer services for hereditary breast/ovarian cancer (HBOC) to outreach areas; however, there has been little research evaluating… (more)

Subjects/Keywords: Cancer; Telehealth; Genetic counselling

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APA (6th Edition):

Zilliacus, E. M. (2010). Evaluating telehealth cancer genetic counselling: impact on genetic counselling outcomes, patient satisfaction and acceptability. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/45526 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8821/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Zilliacus, Elvira Madeleine. “Evaluating telehealth cancer genetic counselling: impact on genetic counselling outcomes, patient satisfaction and acceptability.” 2010. Doctoral Dissertation, University of New South Wales. Accessed December 05, 2019. http://handle.unsw.edu.au/1959.4/45526 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8821/SOURCE01?view=true.

MLA Handbook (7th Edition):

Zilliacus, Elvira Madeleine. “Evaluating telehealth cancer genetic counselling: impact on genetic counselling outcomes, patient satisfaction and acceptability.” 2010. Web. 05 Dec 2019.

Vancouver:

Zilliacus EM. Evaluating telehealth cancer genetic counselling: impact on genetic counselling outcomes, patient satisfaction and acceptability. [Internet] [Doctoral dissertation]. University of New South Wales; 2010. [cited 2019 Dec 05]. Available from: http://handle.unsw.edu.au/1959.4/45526 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8821/SOURCE01?view=true.

Council of Science Editors:

Zilliacus EM. Evaluating telehealth cancer genetic counselling: impact on genetic counselling outcomes, patient satisfaction and acceptability. [Doctoral Dissertation]. University of New South Wales; 2010. Available from: http://handle.unsw.edu.au/1959.4/45526 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8821/SOURCE01?view=true


University of Cape Town

10. Kruger, Brenda Julie. Hereditary nonpolyposis colorectal cancer : factors contributing to adherence and non-adherence to surveillance for mutation carriers in rural areas of the Northern and Western Cape Brenda Julie Kruger.

Degree: Image, Division of Human Genetics, 2005, University of Cape Town

 The aim of this study was to explore possible factors that may affect non-adherence and adherence to surveillance guidelines for mutation positive individuals who are… (more)

Subjects/Keywords: Genetic Counselling

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APA (6th Edition):

Kruger, B. J. (2005). Hereditary nonpolyposis colorectal cancer : factors contributing to adherence and non-adherence to surveillance for mutation carriers in rural areas of the Northern and Western Cape Brenda Julie Kruger. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/3096

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):

Kruger, Brenda Julie. “Hereditary nonpolyposis colorectal cancer : factors contributing to adherence and non-adherence to surveillance for mutation carriers in rural areas of the Northern and Western Cape Brenda Julie Kruger.” 2005. Thesis, University of Cape Town. Accessed December 05, 2019. http://hdl.handle.net/11427/3096.

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

MLA Handbook (7th Edition):

Kruger, Brenda Julie. “Hereditary nonpolyposis colorectal cancer : factors contributing to adherence and non-adherence to surveillance for mutation carriers in rural areas of the Northern and Western Cape Brenda Julie Kruger.” 2005. Web. 05 Dec 2019.

Vancouver:

Kruger BJ. Hereditary nonpolyposis colorectal cancer : factors contributing to adherence and non-adherence to surveillance for mutation carriers in rural areas of the Northern and Western Cape Brenda Julie Kruger. [Internet] [Thesis]. University of Cape Town; 2005. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/11427/3096.

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

Council of Science Editors:

Kruger BJ. Hereditary nonpolyposis colorectal cancer : factors contributing to adherence and non-adherence to surveillance for mutation carriers in rural areas of the Northern and Western Cape Brenda Julie Kruger. [Thesis]. University of Cape Town; 2005. Available from: http://hdl.handle.net/11427/3096

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


University of Sydney

11. Burns, Charlotte. Improving the Clinical Application of Genetic Testing for Patients with Inherited Heart Disease .

Degree: 2019, University of Sydney

 The difficulties associated with the clinical application of next generation sequencing (NGS) approaches can be substantial. However, the technology holds great potential to improve outcomes… (more)

Subjects/Keywords: genetic counselling; inherited heart disease

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APA (6th Edition):

Burns, C. (2019). Improving the Clinical Application of Genetic Testing for Patients with Inherited Heart Disease . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/20321

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):

Burns, Charlotte. “Improving the Clinical Application of Genetic Testing for Patients with Inherited Heart Disease .” 2019. Thesis, University of Sydney. Accessed December 05, 2019. http://hdl.handle.net/2123/20321.

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

MLA Handbook (7th Edition):

Burns, Charlotte. “Improving the Clinical Application of Genetic Testing for Patients with Inherited Heart Disease .” 2019. Web. 05 Dec 2019.

Vancouver:

Burns C. Improving the Clinical Application of Genetic Testing for Patients with Inherited Heart Disease . [Internet] [Thesis]. University of Sydney; 2019. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/2123/20321.

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

Council of Science Editors:

Burns C. Improving the Clinical Application of Genetic Testing for Patients with Inherited Heart Disease . [Thesis]. University of Sydney; 2019. Available from: http://hdl.handle.net/2123/20321

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

12. Düsterwald, Gillian. Understanding doctors' knowledge and attitudes concerning genetics and genetic services in South Africa.

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

 The burgeoning knowledge in genetics implies that genetic services (including clinical and counselling) will be in increasing demand in the future. This study investigated South… (more)

Subjects/Keywords: Genetic Counselling

…the value of genetic services and genetic counselling.. ….59 Fig. 12 Doctors’ responses to… …Foetal alcohol spectrum disorder GC-SA Genetic Counselling South Africa GP General… …and attitudes to genetic services and genetic counselling. The sample population consisted… …Google Scholar database using the terms: [genetic counselling referral OR doctor OR… …genetic counselling to all prospective couples with indications such as family history, a child… 

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APA (6th Edition):

Düsterwald, G. (2015). Understanding doctors' knowledge and attitudes concerning genetics and genetic services in South Africa. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/16487

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):

Düsterwald, Gillian. “Understanding doctors' knowledge and attitudes concerning genetics and genetic services in South Africa.” 2015. Thesis, University of Cape Town. Accessed December 05, 2019. http://hdl.handle.net/11427/16487.

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

MLA Handbook (7th Edition):

Düsterwald, Gillian. “Understanding doctors' knowledge and attitudes concerning genetics and genetic services in South Africa.” 2015. Web. 05 Dec 2019.

Vancouver:

Düsterwald G. Understanding doctors' knowledge and attitudes concerning genetics and genetic services in South Africa. [Internet] [Thesis]. University of Cape Town; 2015. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/11427/16487.

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

Council of Science Editors:

Düsterwald G. Understanding doctors' knowledge and attitudes concerning genetics and genetic services in South Africa. [Thesis]. University of Cape Town; 2015. Available from: http://hdl.handle.net/11427/16487

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

13. Ross, Sinead Amber. Parents' perspectives and experiences of having a child with hereditary hearing loss.

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

 Congenital hearing loss (HL) occurs in 1-2 per 1000 newborns globally. Of all the congenital diseases that occur worldwide, HL remains the most disabling, with… (more)

Subjects/Keywords: Genetic Counselling

…disability and genetic counselling as well as permutations of these terms. The themes extracted… …that is inherited and (3) the role of genetic counselling for hereditary HL. The… …genetic counselling can assist in relieving and normalising feelings of guilt (Kessler et… …IN SOUTH AFRICA AND THE ROLE OF GENETIC COUNSELLING FOR HEREDITARY HEARI NG LOSS It is well… …comprehensive genetics service in SA, which includes diagnosis, genetic counselling and comprehensive… 

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APA (6th Edition):

Ross, S. A. (2016). Parents' perspectives and experiences of having a child with hereditary hearing loss. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/22946

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):

Ross, Sinead Amber. “Parents' perspectives and experiences of having a child with hereditary hearing loss.” 2016. Thesis, University of Cape Town. Accessed December 05, 2019. http://hdl.handle.net/11427/22946.

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

MLA Handbook (7th Edition):

Ross, Sinead Amber. “Parents' perspectives and experiences of having a child with hereditary hearing loss.” 2016. Web. 05 Dec 2019.

Vancouver:

Ross SA. Parents' perspectives and experiences of having a child with hereditary hearing loss. [Internet] [Thesis]. University of Cape Town; 2016. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/11427/22946.

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

Council of Science Editors:

Ross SA. Parents' perspectives and experiences of having a child with hereditary hearing loss. [Thesis]. University of Cape Town; 2016. Available from: http://hdl.handle.net/11427/22946

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


University of Plymouth

14. Lewis, Celine. The effect of psychosocial information resources on the psychological impact of genetic testing for patients.

Degree: PhD, 2011, University of Plymouth

 The effect of psychosocial information resources on the psychological impact of genetic testing for patients Background: The genetic testing process has been shown to have… (more)

Subjects/Keywords: 615.5; genetic testing, genetic counselling, education, patient information, psychosocial, mixed methods

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APA (6th Edition):

Lewis, C. (2011). The effect of psychosocial information resources on the psychological impact of genetic testing for patients. (Doctoral Dissertation). University of Plymouth. Retrieved from http://hdl.handle.net/10026.1/543

Chicago Manual of Style (16th Edition):

Lewis, Celine. “The effect of psychosocial information resources on the psychological impact of genetic testing for patients.” 2011. Doctoral Dissertation, University of Plymouth. Accessed December 05, 2019. http://hdl.handle.net/10026.1/543.

MLA Handbook (7th Edition):

Lewis, Celine. “The effect of psychosocial information resources on the psychological impact of genetic testing for patients.” 2011. Web. 05 Dec 2019.

Vancouver:

Lewis C. The effect of psychosocial information resources on the psychological impact of genetic testing for patients. [Internet] [Doctoral dissertation]. University of Plymouth; 2011. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/10026.1/543.

Council of Science Editors:

Lewis C. The effect of psychosocial information resources on the psychological impact of genetic testing for patients. [Doctoral Dissertation]. University of Plymouth; 2011. Available from: http://hdl.handle.net/10026.1/543


University of Plymouth

15. Godino, Lea. Presymptomatic testing for familial cancer syndromes in young adults : considerations, decision making and impact.

Degree: PhD, 2017, University of Plymouth

 Background: Presymptomatic genetic testing should always involve a considered choice. Young adults are at a key life stage as they may be developing a career,… (more)

Subjects/Keywords: 616.99; genetic counselling; young adults; presymptomatic genetic test; mixed-methods

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APA (6th Edition):

Godino, L. (2017). Presymptomatic testing for familial cancer syndromes in young adults : considerations, decision making and impact. (Doctoral Dissertation). University of Plymouth. Retrieved from http://hdl.handle.net/10026.1/8643

Chicago Manual of Style (16th Edition):

Godino, Lea. “Presymptomatic testing for familial cancer syndromes in young adults : considerations, decision making and impact.” 2017. Doctoral Dissertation, University of Plymouth. Accessed December 05, 2019. http://hdl.handle.net/10026.1/8643.

MLA Handbook (7th Edition):

Godino, Lea. “Presymptomatic testing for familial cancer syndromes in young adults : considerations, decision making and impact.” 2017. Web. 05 Dec 2019.

Vancouver:

Godino L. Presymptomatic testing for familial cancer syndromes in young adults : considerations, decision making and impact. [Internet] [Doctoral dissertation]. University of Plymouth; 2017. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/10026.1/8643.

Council of Science Editors:

Godino L. Presymptomatic testing for familial cancer syndromes in young adults : considerations, decision making and impact. [Doctoral Dissertation]. University of Plymouth; 2017. Available from: http://hdl.handle.net/10026.1/8643


University of Manitoba

16. Dinchong, Rachelle. Reducing the psychosocial impact of a false positive newborn screen for inborn errors of metabolism.

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

 Newborn screening (NBS) is standard practice for neonatal care in Canada and screens for over 20 inborn errors of metabolism (IEM). Education about NBS is… (more)

Subjects/Keywords: newborn screening; inborn errors of metabolism; psychosocial; genetic counselling

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APA (6th Edition):

Dinchong, R. (2019). Reducing the psychosocial impact of a false positive newborn screen for inborn errors of metabolism. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/34019

Chicago Manual of Style (16th Edition):

Dinchong, Rachelle. “Reducing the psychosocial impact of a false positive newborn screen for inborn errors of metabolism.” 2019. Masters Thesis, University of Manitoba. Accessed December 05, 2019. http://hdl.handle.net/1993/34019.

MLA Handbook (7th Edition):

Dinchong, Rachelle. “Reducing the psychosocial impact of a false positive newborn screen for inborn errors of metabolism.” 2019. Web. 05 Dec 2019.

Vancouver:

Dinchong R. Reducing the psychosocial impact of a false positive newborn screen for inborn errors of metabolism. [Internet] [Masters thesis]. University of Manitoba; 2019. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/1993/34019.

Council of Science Editors:

Dinchong R. Reducing the psychosocial impact of a false positive newborn screen for inborn errors of metabolism. [Masters Thesis]. University of Manitoba; 2019. Available from: http://hdl.handle.net/1993/34019


University of New South Wales

17. Saleh, Mona. Cancer, Culture and Genetics: exploring the impact of cultural diversity on the genetic consultation.

Degree: Psychiatry, 2014, University of New South Wales

 This thesis reports on an exploration of the impact cultural and linguistic diversity has on the process of genetic counselling. The first component, the Professional… (more)

Subjects/Keywords: Cultural competence; Cultural diversity; Genetic counselling; Kinship; Hereditary cancer; Genetic services; Arabic-Australians, cultural; Beliefs; Oncology

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APA (6th Edition):

Saleh, M. (2014). Cancer, Culture and Genetics: exploring the impact of cultural diversity on the genetic consultation. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/53453 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12148/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Saleh, Mona. “Cancer, Culture and Genetics: exploring the impact of cultural diversity on the genetic consultation.” 2014. Doctoral Dissertation, University of New South Wales. Accessed December 05, 2019. http://handle.unsw.edu.au/1959.4/53453 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12148/SOURCE02?view=true.

MLA Handbook (7th Edition):

Saleh, Mona. “Cancer, Culture and Genetics: exploring the impact of cultural diversity on the genetic consultation.” 2014. Web. 05 Dec 2019.

Vancouver:

Saleh M. Cancer, Culture and Genetics: exploring the impact of cultural diversity on the genetic consultation. [Internet] [Doctoral dissertation]. University of New South Wales; 2014. [cited 2019 Dec 05]. Available from: http://handle.unsw.edu.au/1959.4/53453 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12148/SOURCE02?view=true.

Council of Science Editors:

Saleh M. Cancer, Culture and Genetics: exploring the impact of cultural diversity on the genetic consultation. [Doctoral Dissertation]. University of New South Wales; 2014. Available from: http://handle.unsw.edu.au/1959.4/53453 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12148/SOURCE02?view=true


University of Manitoba

18. Krutish, Angela. Exploration of the genetic assistant position in the provision of genetics services.

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

Genetic counsellors (GCs) are healthcare professionals with specialized training in genetics and counselling. There are approximately 4,000 certified GCs in North America; however, this is… (more)

Subjects/Keywords: Genetic assistant; Genetic counselling; Health workforce; Health human resource; Role substitution; Skill-management; Staff-mix; Genetics

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

APA (6th Edition):

Krutish, A. (2019). Exploration of the genetic assistant position in the provision of genetics services. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/34020

Chicago Manual of Style (16th Edition):

Krutish, Angela. “Exploration of the genetic assistant position in the provision of genetics services.” 2019. Masters Thesis, University of Manitoba. Accessed December 05, 2019. http://hdl.handle.net/1993/34020.

MLA Handbook (7th Edition):

Krutish, Angela. “Exploration of the genetic assistant position in the provision of genetics services.” 2019. Web. 05 Dec 2019.

Vancouver:

Krutish A. Exploration of the genetic assistant position in the provision of genetics services. [Internet] [Masters thesis]. University of Manitoba; 2019. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/1993/34020.

Council of Science Editors:

Krutish A. Exploration of the genetic assistant position in the provision of genetics services. [Masters Thesis]. University of Manitoba; 2019. Available from: http://hdl.handle.net/1993/34020


University of Manitoba

19. Hansen, Ashleigh. Exploring immigrants’ perceptions of genetic counselling.

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

 There has been a steady increase in immigration to Manitoba. Several studies have shown that immigrants face barriers when accessing health care services, such as… (more)

Subjects/Keywords: Immigrants; Canada; Canadian immigrants; Newcomer; Refugee; Canadian refugee; Health care access; Barriers to health care; Genetic counselling; Genetic; Service delivery

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

APA (6th Edition):

Hansen, A. (2019). Exploring immigrants’ perceptions of genetic counselling. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/34159

Chicago Manual of Style (16th Edition):

Hansen, Ashleigh. “Exploring immigrants’ perceptions of genetic counselling.” 2019. Masters Thesis, University of Manitoba. Accessed December 05, 2019. http://hdl.handle.net/1993/34159.

MLA Handbook (7th Edition):

Hansen, Ashleigh. “Exploring immigrants’ perceptions of genetic counselling.” 2019. Web. 05 Dec 2019.

Vancouver:

Hansen A. Exploring immigrants’ perceptions of genetic counselling. [Internet] [Masters thesis]. University of Manitoba; 2019. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/1993/34159.

Council of Science Editors:

Hansen A. Exploring immigrants’ perceptions of genetic counselling. [Masters Thesis]. University of Manitoba; 2019. Available from: http://hdl.handle.net/1993/34159


University of Adelaide

20. Thompson, Elizabeth Mary, 1953-. Genetic counselling in severe osteogenesis imperfecta / by Elizabeth Mary Thompson.

Degree: 1990, University of Adelaide

Addresses the problem of giving genetic counselling to parents of a "sporadic" case of severe osteogenesis imperfecta, either of the perinatally lethal or severe deforming variety. Advisors/Committee Members: Dept. of Paediatrics (school).

Subjects/Keywords: 616.71/042 616/.042 20; Osteogenesis imperfecta Genetic aspects; Genetic disorders; Genetic counselling

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APA (6th Edition):

Thompson, Elizabeth Mary, 1. (1990). Genetic counselling in severe osteogenesis imperfecta / by Elizabeth Mary Thompson. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/38438

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):

Thompson, Elizabeth Mary, 1953-. “Genetic counselling in severe osteogenesis imperfecta / by Elizabeth Mary Thompson.” 1990. Thesis, University of Adelaide. Accessed December 05, 2019. http://hdl.handle.net/2440/38438.

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

MLA Handbook (7th Edition):

Thompson, Elizabeth Mary, 1953-. “Genetic counselling in severe osteogenesis imperfecta / by Elizabeth Mary Thompson.” 1990. Web. 05 Dec 2019.

Vancouver:

Thompson, Elizabeth Mary 1. Genetic counselling in severe osteogenesis imperfecta / by Elizabeth Mary Thompson. [Internet] [Thesis]. University of Adelaide; 1990. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/2440/38438.

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

Council of Science Editors:

Thompson, Elizabeth Mary 1. Genetic counselling in severe osteogenesis imperfecta / by Elizabeth Mary Thompson. [Thesis]. University of Adelaide; 1990. Available from: http://hdl.handle.net/2440/38438

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


Vilnius University

21. Utkus, Algirdas. Retosios ligos, jų fenomika ir genetinis konsultavimas.

Degree: Review of scientific papers submitted for habilitation procedure, Medicine, 2009, Vilnius University

Retosios ligos (RL) – tai ypač mažai paplitusios ligos (gyvybei pavojų keliančios arba lėtai sekinančios ligos), kuriomis Europos Sąjungoje (ES) serga ne daugiau kaip 5… (more)

Subjects/Keywords: Retosios ligos; Įgimtos anomalijos; Fenomika; Genetinis konsultavimas; Fliuktacinė asimetrija; Rare diseases; Congenital anomalies; Phenomics; Genetic counselling; Fluctuating asymmetry

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

APA (6th Edition):

Utkus, A. (2009). Retosios ligos, jų fenomika ir genetinis konsultavimas. (Thesis). Vilnius University. Retrieved from http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2009~D_20090526_111352-29090 ;

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):

Utkus, Algirdas. “Retosios ligos, jų fenomika ir genetinis konsultavimas.” 2009. Thesis, Vilnius University. Accessed December 05, 2019. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2009~D_20090526_111352-29090 ;.

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

MLA Handbook (7th Edition):

Utkus, Algirdas. “Retosios ligos, jų fenomika ir genetinis konsultavimas.” 2009. Web. 05 Dec 2019.

Vancouver:

Utkus A. Retosios ligos, jų fenomika ir genetinis konsultavimas. [Internet] [Thesis]. Vilnius University; 2009. [cited 2019 Dec 05]. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2009~D_20090526_111352-29090 ;.

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

Council of Science Editors:

Utkus A. Retosios ligos, jų fenomika ir genetinis konsultavimas. [Thesis]. Vilnius University; 2009. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2009~D_20090526_111352-29090 ;

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


University of Gothenburg / Göteborgs Universitet

22. Järvholm, Stina. “It is better to have tried, no matter what” : Psychological perspectives on pre-implantation genetic diagnosis (PGD).

Degree: 2017, University of Gothenburg / Göteborgs Universitet

 Couples with the risk of transmitting a genetic disease face different diagnostic options when they wish to become parents. Pre-implantation genetic diagnosis (PGD) combines in… (more)

Subjects/Keywords: Pre-implantation Genetic Diagnosis (PGD); Decision-making; Men and Women; Risk Factors; Depression; Anxiety; Marital Relationship; Counselling

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APA (6th Edition):

Järvholm, S. (2017). “It is better to have tried, no matter what” : Psychological perspectives on pre-implantation genetic diagnosis (PGD). (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/51960

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):

Järvholm, Stina. ““It is better to have tried, no matter what” : Psychological perspectives on pre-implantation genetic diagnosis (PGD).” 2017. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed December 05, 2019. http://hdl.handle.net/2077/51960.

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

MLA Handbook (7th Edition):

Järvholm, Stina. ““It is better to have tried, no matter what” : Psychological perspectives on pre-implantation genetic diagnosis (PGD).” 2017. Web. 05 Dec 2019.

Vancouver:

Järvholm S. “It is better to have tried, no matter what” : Psychological perspectives on pre-implantation genetic diagnosis (PGD). [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2017. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/2077/51960.

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

Council of Science Editors:

Järvholm S. “It is better to have tried, no matter what” : Psychological perspectives on pre-implantation genetic diagnosis (PGD). [Thesis]. University of Gothenburg / Göteborgs Universitet; 2017. Available from: http://hdl.handle.net/2077/51960

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


Massey University

23. Mann, Heather M. Double Epistemologies and ‘Respons-ability’ in Public Healthcare: Talanoa with Tongans in New Zealand.

Degree: MA, Social Anthropology, 2017, Massey University

 Pacific health policy in Aotearoa/New Zealand focuses on reducing health inequities between the majority population and Pacific Islander communities. At the same time, the public… (more)

Subjects/Keywords: Tongans; Health and hygiene; Services for; Social life and customs; Genetic counselling; Social aspects; New Zealand

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APA (6th Edition):

Mann, H. M. (2017). Double Epistemologies and ‘Respons-ability’ in Public Healthcare: Talanoa with Tongans in New Zealand. (Masters Thesis). Massey University. Retrieved from http://hdl.handle.net/10179/13581

Chicago Manual of Style (16th Edition):

Mann, Heather M. “Double Epistemologies and ‘Respons-ability’ in Public Healthcare: Talanoa with Tongans in New Zealand.” 2017. Masters Thesis, Massey University. Accessed December 05, 2019. http://hdl.handle.net/10179/13581.

MLA Handbook (7th Edition):

Mann, Heather M. “Double Epistemologies and ‘Respons-ability’ in Public Healthcare: Talanoa with Tongans in New Zealand.” 2017. Web. 05 Dec 2019.

Vancouver:

Mann HM. Double Epistemologies and ‘Respons-ability’ in Public Healthcare: Talanoa with Tongans in New Zealand. [Internet] [Masters thesis]. Massey University; 2017. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/10179/13581.

Council of Science Editors:

Mann HM. Double Epistemologies and ‘Respons-ability’ in Public Healthcare: Talanoa with Tongans in New Zealand. [Masters Thesis]. Massey University; 2017. Available from: http://hdl.handle.net/10179/13581


Universitat Pompeu Fabra

24. Reina Castillón, Judith, 1989-. Detectable clonal mosaicism : underlying mechanisms, clinical implications and genetic counselling.

Degree: Departament de Ciències Experimentals i de la Salut, 2017, Universitat Pompeu Fabra

 El mosaicisme genètic somàtic pot està present en individus sans i en altres amb certes condicions com edat avançada o càncer. La seva detecció en… (more)

Subjects/Keywords: Clonal mosaicism; Fanconi anemia; Chronic lymphothytic leukemia; Rescue uniparental disomy; Genetic counselling; Mosaicisme clonal; Anemia de Fanconi; Leucèmia linfocítica crònica; Disomia uniparental de rescat; Assessorament genetic; 575

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APA (6th Edition):

Reina Castillón, Judith, 1. (2017). Detectable clonal mosaicism : underlying mechanisms, clinical implications and genetic counselling. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/666707

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):

Reina Castillón, Judith, 1989-. “Detectable clonal mosaicism : underlying mechanisms, clinical implications and genetic counselling.” 2017. Thesis, Universitat Pompeu Fabra. Accessed December 05, 2019. http://hdl.handle.net/10803/666707.

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

MLA Handbook (7th Edition):

Reina Castillón, Judith, 1989-. “Detectable clonal mosaicism : underlying mechanisms, clinical implications and genetic counselling.” 2017. Web. 05 Dec 2019.

Vancouver:

Reina Castillón, Judith 1. Detectable clonal mosaicism : underlying mechanisms, clinical implications and genetic counselling. [Internet] [Thesis]. Universitat Pompeu Fabra; 2017. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/10803/666707.

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

Council of Science Editors:

Reina Castillón, Judith 1. Detectable clonal mosaicism : underlying mechanisms, clinical implications and genetic counselling. [Thesis]. Universitat Pompeu Fabra; 2017. Available from: http://hdl.handle.net/10803/666707

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


Universidade do Rio Grande do Sul

25. Santos, João Paulo Franco dos. Prevalência de critérios para avaliação genética em pacientes com câncer de mama atendidos no hospital universitário de Santa Maria.

Degree: 2016, Universidade do Rio Grande do Sul

Objetivo: Até 10% dos casos de câncer de mama estão associados com uma síndrome genética de predisposição ao câncer. A identificação de possíveis portadores dessas… (more)

Subjects/Keywords: Breast cancer; Síndrome de Li-Fraumeni; Neoplasias da mama; Genetic counselling; Hereditary cancer syndromes; Hereditary breast and ovarian cancer syndrome; Li-Fraumeni syndrome

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APA (6th Edition):

Santos, J. P. F. d. (2016). Prevalência de critérios para avaliação genética em pacientes com câncer de mama atendidos no hospital universitário de Santa Maria. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/143202

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):

Santos, João Paulo Franco dos. “Prevalência de critérios para avaliação genética em pacientes com câncer de mama atendidos no hospital universitário de Santa Maria.” 2016. Thesis, Universidade do Rio Grande do Sul. Accessed December 05, 2019. http://hdl.handle.net/10183/143202.

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

MLA Handbook (7th Edition):

Santos, João Paulo Franco dos. “Prevalência de critérios para avaliação genética em pacientes com câncer de mama atendidos no hospital universitário de Santa Maria.” 2016. Web. 05 Dec 2019.

Vancouver:

Santos JPFd. Prevalência de critérios para avaliação genética em pacientes com câncer de mama atendidos no hospital universitário de Santa Maria. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2016. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/10183/143202.

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

Council of Science Editors:

Santos JPFd. Prevalência de critérios para avaliação genética em pacientes com câncer de mama atendidos no hospital universitário de Santa Maria. [Thesis]. Universidade do Rio Grande do Sul; 2016. Available from: http://hdl.handle.net/10183/143202

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


Linköping University

26. Smolska, Andriana. Selective abortion on the basis of prenatal genetic diagnosis: ethical problems faced by the doctor.

Degree: Centre for Applied Ethics, 2006, Linköping University

  The modern world is facing a revolutionary development in the clinical medicine and biomedical sciences. Due to the different life supporting systems, it is… (more)

Subjects/Keywords: Prenatal genetic diagnosis; selective abortion; fetus; medical counselling; Philosophy subjects; Filosofiämnen

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APA (6th Edition):

Smolska, A. (2006). Selective abortion on the basis of prenatal genetic diagnosis: ethical problems faced by the doctor. (Thesis). Linköping University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-6683

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):

Smolska, Andriana. “Selective abortion on the basis of prenatal genetic diagnosis: ethical problems faced by the doctor.” 2006. Thesis, Linköping University. Accessed December 05, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-6683.

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

MLA Handbook (7th Edition):

Smolska, Andriana. “Selective abortion on the basis of prenatal genetic diagnosis: ethical problems faced by the doctor.” 2006. Web. 05 Dec 2019.

Vancouver:

Smolska A. Selective abortion on the basis of prenatal genetic diagnosis: ethical problems faced by the doctor. [Internet] [Thesis]. Linköping University; 2006. [cited 2019 Dec 05]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-6683.

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

Council of Science Editors:

Smolska A. Selective abortion on the basis of prenatal genetic diagnosis: ethical problems faced by the doctor. [Thesis]. Linköping University; 2006. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-6683

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


University of New South Wales

27. Morrigan, Viviane. An ethics of reproductive choice : genetic counselling and prenatal diagnosis.

Degree: History & Philosophy of Science, 2002, University of New South Wales

 For this project I describe the socio-historical development of a particularapplication of genetic prenatal diagnosis, in terms of changing social relationsthat govern an ethics of… (more)

Subjects/Keywords: Human reproduction  – Moral and ethical aspects; Genetic counselling; Prenatal diagnosis

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

APA (6th Edition):

Morrigan, V. (2002). An ethics of reproductive choice : genetic counselling and prenatal diagnosis. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/19396 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:597/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Morrigan, Viviane. “An ethics of reproductive choice : genetic counselling and prenatal diagnosis.” 2002. Doctoral Dissertation, University of New South Wales. Accessed December 05, 2019. http://handle.unsw.edu.au/1959.4/19396 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:597/SOURCE01?view=true.

MLA Handbook (7th Edition):

Morrigan, Viviane. “An ethics of reproductive choice : genetic counselling and prenatal diagnosis.” 2002. Web. 05 Dec 2019.

Vancouver:

Morrigan V. An ethics of reproductive choice : genetic counselling and prenatal diagnosis. [Internet] [Doctoral dissertation]. University of New South Wales; 2002. [cited 2019 Dec 05]. Available from: http://handle.unsw.edu.au/1959.4/19396 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:597/SOURCE01?view=true.

Council of Science Editors:

Morrigan V. An ethics of reproductive choice : genetic counselling and prenatal diagnosis. [Doctoral Dissertation]. University of New South Wales; 2002. Available from: http://handle.unsw.edu.au/1959.4/19396 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:597/SOURCE01?view=true


Tampere University

28. Mälkiä, Tiina. Moraalia vai lääketiedettä? Kuinka sikiödiagnostiikasta ja selektiivisestä abortista puhutaan perinnöllisyysneuvonnassa .

Degree: Sosiologian ja sosiaalipsykologian laitos - Department of Sociology and Social Psychology, 2008, Tampere University

 Ihmisen perimää koskevan tiedon lisääntyessä tarvitaan myös keskustelua siitä, miten lääketieteen kehitys, yhteiskunnan ja yksilön edut, arvot ja moraalikäsitykset sovitetaan yhteen. Perinnöllisiä sairauksia koskevan tiedon… (more)

Subjects/Keywords: perinnöllisyysneuvonta; moraali; keskustelunanalyysi; ohjailemattomuus; genetic counselling; morality; conversation analysis; nondirectiveness

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

APA (6th Edition):

Mälkiä, T. (2008). Moraalia vai lääketiedettä? Kuinka sikiödiagnostiikasta ja selektiivisestä abortista puhutaan perinnöllisyysneuvonnassa . (Doctoral Dissertation). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/66408

Chicago Manual of Style (16th Edition):

Mälkiä, Tiina. “Moraalia vai lääketiedettä? Kuinka sikiödiagnostiikasta ja selektiivisestä abortista puhutaan perinnöllisyysneuvonnassa .” 2008. Doctoral Dissertation, Tampere University. Accessed December 05, 2019. https://trepo.tuni.fi/handle/10024/66408.

MLA Handbook (7th Edition):

Mälkiä, Tiina. “Moraalia vai lääketiedettä? Kuinka sikiödiagnostiikasta ja selektiivisestä abortista puhutaan perinnöllisyysneuvonnassa .” 2008. Web. 05 Dec 2019.

Vancouver:

Mälkiä T. Moraalia vai lääketiedettä? Kuinka sikiödiagnostiikasta ja selektiivisestä abortista puhutaan perinnöllisyysneuvonnassa . [Internet] [Doctoral dissertation]. Tampere University; 2008. [cited 2019 Dec 05]. Available from: https://trepo.tuni.fi/handle/10024/66408.

Council of Science Editors:

Mälkiä T. Moraalia vai lääketiedettä? Kuinka sikiödiagnostiikasta ja selektiivisestä abortista puhutaan perinnöllisyysneuvonnassa . [Doctoral Dissertation]. Tampere University; 2008. Available from: https://trepo.tuni.fi/handle/10024/66408


Universitat Autònoma de Barcelona

29. Esteban Marcos, Irene. Aplicación clínica de los paneles de genes de susceptibilidad al cáncer: caracterización de variantes en genes de riesgo e impacto psicológico.

Degree: Departament de Genètica i de Microbiologia, 2019, Universitat Autònoma de Barcelona

 Introduction: Hereditary cancer panels are currently being incorporated into clinical practice. These panels can include genes associated with different types of cancer and different levels… (more)

Subjects/Keywords: Càncer hereditari; Cáncer hereditario; Hereditary cancer; Panells de gens; Paneles de genes; Multigene panels; Assessorament genètic; Aseoramiento genético; Genetic counselling; Ciències Experimentals; 575

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

APA (6th Edition):

Esteban Marcos, I. (2019). Aplicación clínica de los paneles de genes de susceptibilidad al cáncer: caracterización de variantes en genes de riesgo e impacto psicológico. (Thesis). Universitat Autònoma de Barcelona. Retrieved from http://hdl.handle.net/10803/667408

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):

Esteban Marcos, Irene. “Aplicación clínica de los paneles de genes de susceptibilidad al cáncer: caracterización de variantes en genes de riesgo e impacto psicológico.” 2019. Thesis, Universitat Autònoma de Barcelona. Accessed December 05, 2019. http://hdl.handle.net/10803/667408.

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

MLA Handbook (7th Edition):

Esteban Marcos, Irene. “Aplicación clínica de los paneles de genes de susceptibilidad al cáncer: caracterización de variantes en genes de riesgo e impacto psicológico.” 2019. Web. 05 Dec 2019.

Vancouver:

Esteban Marcos I. Aplicación clínica de los paneles de genes de susceptibilidad al cáncer: caracterización de variantes en genes de riesgo e impacto psicológico. [Internet] [Thesis]. Universitat Autònoma de Barcelona; 2019. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/10803/667408.

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

Council of Science Editors:

Esteban Marcos I. Aplicación clínica de los paneles de genes de susceptibilidad al cáncer: caracterización de variantes en genes de riesgo e impacto psicológico. [Thesis]. Universitat Autònoma de Barcelona; 2019. Available from: http://hdl.handle.net/10803/667408

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

30. Dijk, Sandra van. Chances and changes: psychological impact of genetic counselling and DNA testing for breast cancer.

Degree: 2006, Department of Medical Decision Making, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University

 The cumulative lifetime risk of developing breast cancer for a Dutch woman is about 12%. In some families breast cancer seems to occur even more… (more)

Subjects/Keywords: BRCA; Breast cancer; Distress; DNA-test; Genetic counselling; Impact; Psychological; Risk perception; BRCA; Breast cancer; Distress; DNA-test; Genetic counselling; Impact; Psychological; Risk perception

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

APA (6th Edition):

Dijk, S. v. (2006). Chances and changes: psychological impact of genetic counselling and DNA testing for breast cancer. (Doctoral Dissertation). Department of Medical Decision Making, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/4989

Chicago Manual of Style (16th Edition):

Dijk, Sandra van. “Chances and changes: psychological impact of genetic counselling and DNA testing for breast cancer.” 2006. Doctoral Dissertation, Department of Medical Decision Making, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Accessed December 05, 2019. http://hdl.handle.net/1887/4989.

MLA Handbook (7th Edition):

Dijk, Sandra van. “Chances and changes: psychological impact of genetic counselling and DNA testing for breast cancer.” 2006. Web. 05 Dec 2019.

Vancouver:

Dijk Sv. Chances and changes: psychological impact of genetic counselling and DNA testing for breast cancer. [Internet] [Doctoral dissertation]. Department of Medical Decision Making, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2006. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/1887/4989.

Council of Science Editors:

Dijk Sv. Chances and changes: psychological impact of genetic counselling and DNA testing for breast cancer. [Doctoral Dissertation]. Department of Medical Decision Making, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2006. Available from: http://hdl.handle.net/1887/4989

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