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 Feben, C, Kromberg, J and Krause, A An unusual case of Trisomy 13. S. Afr. j. child health, Apr 2015, vol.9, no.2, p.61-62. ISSN 1999-7671
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 van Wyk, C et al. Knowledge regarding basic concepts of hereditary cancers, and the available genetic counselling and testing services: A survey of general practitioners in Johannesburg, South Africa. SAMJ, S. Afr. med. j., Mar 2016, vol.106, no.3, p.268-271. ISSN 0256-9574
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 Seymour, H J et al. Breast cancer in high-risk Afrikaner families: Is BRCA founder mutation testing sufficient?. SAMJ, S. Afr. med. j., Mar 2016, vol.106, no.3, p.264-267. ISSN 0256-9574
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 Magazi, D S et al. Huntington's disease: Genetic heterogeneity in black African patients. SAMJ, S. Afr. med. j., Mar 2008, vol.98, no.3, p.200-203. ISSN 0256-9574
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 Kerr, R et al. Genetic testing for Duchenne/Becker muscular dystrophy in Johannesburg, South Africa. SAMJ, S. Afr. med. j., Dec 2013, vol.103, no.12, p.999-1004. ISSN 0256-9574
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 Essop, F B and Krause, A Diagnostic, carrier and prenatal genetic testing for fragile X syndrome and other FMR-l-related disorders in Johannesburg, South Africa: A 20-year review. SAMJ, S. Afr. med. j., Dec 2013, vol.103, no.12, p.994-998. ISSN 0256-9574
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 Krause, A et al. Testing for haemoglobinopathies in Johannesburg, South Africa: A 30-year review. SAMJ, S. Afr. med. j., Dec 2013, vol.103, no.12, p.989-993. ISSN 0256-9574
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 Teckie, G, Krause, A and Kromberg, J G R Neural tube defects in Gauteng, South Africa: Recurrence risks and associated factors. SAMJ, S. Afr. med. j., Dec 2013, vol.103, no.12, p.973-977. ISSN 0256-9574
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 Wainstein, T et al. Fanconi anaemia in black South African patients heterozygous for the FANCG c.637-643delTACCGCC founder mutation. SAMJ, S. Afr. med. j., Dec 2013, vol.103, no.12, p.970-973. ISSN 0256-9574
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 Kromberg, J G R and Krause, A Human genetics in Johannesburg, South Africa: Past, present and future. SAMJ, S. Afr. med. j., Dec 2013, vol.103, no.12, p.957-961. ISSN 0256-9574
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