Channels :: FRELIP Discovery

Author: Wessels, Tina-Marie

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At-risk individual's perspectives of Spinocerebellar Ataxia (SCA) Presymptomatic Testing (PT)

Similar Items: At-risk individual's perspectives of Spinocerebellar Ataxia (SCA) Presymptomatic Testing (PT)

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Spinocerebellar ataxias
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Spinocerebellar ataxia type 7 in southern africa: an epidemiological, molecular and cellular study
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An intronic variant in Ferredoxin Reductase (FDXR) creates a cryptic exon in Quarter Horses with Equine Juvenile Spinocerebellar Ataxia
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Novel cell models for the study of spinocerebellar ataxia type 7 pathogenesis and therapy in a South African patient cohort
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Perspectives and Experiences of Individuals Undergoing Predictive Testing for Hereditary Breast and Ovarian Cancer (HBOC) Syndrome in the Western Cape, South Africa.
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Returning individual genetic results to research participants: experiences of stigma in South African families with neurodevelopmental disorders
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Return of a Fragile X Syndrome Genetic Result: Exploring the feedback of Individual genetic findings and their relation to traditional knowledge in a village in Cameroon
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Exploring the Experiences and Perceptions of Individuals who have Completed the Discovery Health Family History Tool, and how the Personalised Report has Impacted their Lives
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Parents' perspectives and experiences of having a child with hereditary hearing loss
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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
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The use of precision medicine on children with refractory epilepsy in South Africa: Caregivers’ experiences, perspectives and expectations
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Development of a SCA7 patient-derived lymphoblast cell model for testing RNAi knock-down of the disease-causing gene
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The role of a genetic counsellor in a support group for Huntington disease
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Understanding doctors' knowledge and attitudes concerning genetics and genetic services in South Africa
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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.
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Exploration of the impact of genetic counselling and patient support group involvement on retinal degenerative disorders (RDD) patients: a qualitative study
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Investigating the views and experiences of Fetal Medicine Practitioners offering late termination of pregnancy in the Western Cape
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Women's experiences of receiving a child's fetal alcohol spectrum disorder diagnosis: a Western Cape study
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Knowledge and experiences of parents with children affected by Sickle Cell Disease in Cape Town
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The experiences of couples undergoing Preimplantation Genetic Diagnosis (PGD) at the Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital (SQUH) in Oman
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Exploring the decision making process of women offered termination of pregnancy for serious congenital abnormality
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The factors affecting the inherited retinal disease project in South Africa - Including insights from Genetic Counsellors
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Perceptions of health-related quality of life among adults living with sickle cell disease in Cape Town, South Africa
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Medical Practitioners' use of genetic counselling services in Cape Town