Krause A - Search Results

1

Breast cancer in high-risk Afrikaner families: Is BRCA founder mutation testing sufficient?

Seymour HJ, Wainstein T, Macaulay S, Haw T, Krause A. Seymour HJ, et al. Among authors: krause a. S Afr Med J. 2016 Feb 3;106(3):264-7. doi: 10.7196/SAMJ.2016.v106i3.10285. S Afr Med J. 2016. PMID: 26915939

2

Utilisation of predictive, prenatal and diagnostic testing for Huntington's disease in Johannesburg.

Kromberg JG, Krause A, Spurdle AB, Temlett JA, Lucas M, Rodseth D, Stevens G, Jenkins T. Kromberg JG, et al. Among authors: krause a. S Afr Med J. 1999 Jul;89(7):774-8. S Afr Med J. 1999. PMID: 10470316

3

The utilization and outcome of diagnostic, predictive, and prenatal genetic testing for huntington disease in johannesburg, South Africa.

Sizer EB, Haw T, Wessels TM, Kromberg JG, Krause A. Sizer EB, et al. Among authors: krause a. Genet Test Mol Biomarkers. 2012 Jan;16(1):58-62. doi: 10.1089/gtmb.2011.0007. Epub 2011 Aug 12. Genet Test Mol Biomarkers. 2012. PMID: 21838519

4

Phenotypic consequences in black South African Fanconi anemia patients homozygous for a founder mutation.

Feben C, Kromberg J, Wainwright R, Stones D, Sutton C, Poole J, Haw T, Krause A. Feben C, et al. Among authors: krause a. Genet Med. 2014 May;16(5):400-6. doi: 10.1038/gim.2013.159. Epub 2013 Oct 17. Genet Med. 2014. PMID: 24136620 Free article.

5

Human genetics in Johannesburg, South Africa: past, present and future.

Kromberg JG, Krause A. Kromberg JG, et al. Among authors: krause a. S Afr Med J. 2013 Oct 11;103(12 Suppl 1):957-61. doi: 10.7196/samj.7220. S Afr Med J. 2013. PMID: 24300637

6

Fanconi anaemia in black South African patients heterozygous for the FANCG c.637-643delTACCGCC founder mutation.

Wainstein T, Kerr R, Mitchell CL, Madaree S, Essop FB, Vorster E, Wainwright R, Poole J, Krause A. Wainstein T, et al. Among authors: krause a. S Afr Med J. 2013 Oct 11;103(12 Suppl 1):970-3. doi: 10.7196/samj.7215. S Afr Med J. 2013. PMID: 24300640

7

Neural tube defects in Gauteng, South Africa: recurrence risks and associated factors.

Teckie G, Krause A, Kromberg JG. Teckie G, et al. Among authors: krause a. S Afr Med J. 2013 Sep 17;103(12 Suppl 1):973-7. doi: 10.7196/samj.7119. S Afr Med J. 2013. PMID: 24300641

8

Testing for haemoglobinopathies in Johannesburg, South Africa: a 30-year review.

Krause A, Wainstein T, Essop FB, Goodyear Q. Krause A, et al. S Afr Med J. 2013 Oct 11;103(12 Suppl 1):989-93. doi: 10.7196/samj.7255. S Afr Med J. 2013. PMID: 24300645

9

Diagnostic, carrier and prenatal genetic testing for fragile X syndrome and other FMR-1-related disorders in Johannesburg, South Africa: a 20-year review.

Essop FB, Krause A. Essop FB, et al. Among authors: krause a. S Afr Med J. 2013 Oct 11;103(12 Suppl 1):994-8. doi: 10.7196/samj.7144. S Afr Med J. 2013. PMID: 24300646

10

Genetic testing for Duchenne/Becker muscular dystrophy in Johannesburg, South Africa.

Kerr R, Robinson C, Essop FB, Krause A. Kerr R, et al. Among authors: krause a. S Afr Med J. 2013 Oct 10;103(12 Suppl 1):999-1004. doi: 10.7196/samj.7274. S Afr Med J. 2013. PMID: 24300647

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