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Search on :	KRAUSE, A [Author]
References found :	18 [refine]
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Feben, C et al. Timely diagnosis of vascular Ehlers Danlos syndrome - the need for genetic testing and counselling. S. Afr. j. surg., Sept 2018, vol.56, no.3, p.30-33. ISSN 0038-2361

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Spencer, C E et al. Diandric triploidy in a liveborn infant with 3-4 syndactyly and a neural tube defect. S. Afr. j. child health, Dec 2017, vol.11, no.4, p.198-200. ISSN 1999-7671

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Feben, C et al. Fanconi anaemia in South African patients with Afrikaner ancestry. S. Afr. j. child health, Oct 2017, vol.11, no.3, p.141-145. ISSN 1999-7671

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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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Alii, N A et al. Thalassaemia (part 1). SAMJ, S. Afr. med. j., June 2021, vol.111, no.6, p.529-534. ISSN 0256-9574

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Bailly, C et al. Role of family history and clinical screening in the identification of families with idiopathic dilated cardiomyopathy in Johannesburg, South Africa. SAMJ, S. Afr. med. j., Sept 2019, vol.109, no.9, p.673-678. ISSN 0256-9574

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Krause, A. New genetic testing technologies: Advantages and limitations. SAMJ, S. Afr. med. j., Apr 2019, vol.109, no.4, p.207-209. ISSN 0256-9574

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Feben, C et al. Fanconi anaemia in South Africa: Past, present and future. SAMJ, S. Afr. med. j., May 2018, vol.108, no.5, p.393-398. ISSN 0256-9574

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Mudau, M M, Essop, F and Krause, A A novel FKRP-related muscular dystrophy founder mutation in South African Afrikaner patients with a phenotype suggestive of a dystrophinopathy. SAMJ, S. Afr. med. j., Jan 2017, vol.107, no.1, p.80-82. ISSN 0256-9574

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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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