Development of a SCA7 patient-derived lymphoblast cell model for testing RNAi knock-down of the disease-causing gene by Berkowitz, Danielle Claire

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Spinocerebellar ataxia type 7 in southern africa: an epidemiological, molecular and cellular study by Smith, Danielle Claire

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A molecular investigation of Huntington disease; origins of the mutation and current prevalence in South Africa by Baine, Fiona Eugenie Kebirungi

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A molecular investigation of the novel gene underlying autosomal dominant retinitis pigmentosa in a South African family by Bardien-Kruger, Soraya

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

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Towards identifying the ADRP gene in a large South African family with retinitis pigmentosa by Goliath, René

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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 Cap... by Kruger, Brenda Julie

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RNAi based allele-specific silencing of the disease-causing gene in black South African patients with SCA7 by Scholefield, Janine

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The molecular investigation of Stargardt disease in South Africa by September, Alison

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Novel cell models for the study of spinocerebellar ataxia type 7 pathogenesis and therapy in a South African patient cohort by Watson, Lauren

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Apoptosis in Haematopoietic progenitors by Rossouw, Sophia Catherine

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An investigation into the understanding of basic genetic inheritance amongst amaXhosa caregivers of patients with Haemophilia by Solomon, Gabriele Anna Eva

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A pilot study of how individuals with inherited retinal degenerative disorders perceived being part of a genetic research programme by Basson, Frieda

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The genetic basis of human athletic performance by Bekker, Jan Pieter Ignatius

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An investigation into the level of genetic knowledge of parents of sons with Duchenne Muscular Dystrophy and their satisfaction with the genetic counselling service at Red Cross Wa... by Loggenberg, Kelly

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Detailed investigation of the unstable (CAG) repeat and the immediate surrounding region of the IT15 gene in some South African families with Huntington disease by Scholefield, Janine

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Mutation analysis of important retinal candidate genes: progression from research to diagnostic service by Roberts, Lisa Jane

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