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

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text

Apoptosis in Haematopoietic progenitors by Rossouw, Sophia Catherine

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text

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

Get full text