Channels :: FRELIP Discovery

Author: Wonkam, Ambroise

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Knowledge and experiences of parents with children affected by Sickle Cell Disease in Cape Town

Similar Items: Knowledge and experiences of parents with children affected by Sickle Cell Disease in Cape Town

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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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Parents' perspectives and experiences of having a child with hereditary hearing loss
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Parental perceptions of the educational needs of children with genetic conditions leading to intellectual disabilities
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The factors affecting the inherited retinal disease project in South Africa - Including insights from Genetic Counsellors
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Medical Practitioners' use of genetic counselling services in Cape Town
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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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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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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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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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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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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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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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Sickle cell trait and targeted genomic variants in chronic kidney disease an African cohort
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Study of genetic modifiers of fetal hemoglobin and mechanisms of hydroxyurea-induced γ-globin expression in sickle cell disease
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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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At-risk individual's perspectives of Spinocerebellar Ataxia (SCA) Presymptomatic Testing (PT)
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Exploring the decision making process of women offered termination of pregnancy for serious congenital abnormality