Krause A - Search Results

1

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.

2

A new high activity plasma cholinesterase variant.

Krause A, Lane AB, Jenkins T. Krause A, et al. J Med Genet. 1988 Oct;25(10):677-81. doi: 10.1136/jmg.25.10.677. J Med Genet. 1988. PMID: 3225823 Free PMC article.

3

Waardenburg syndrome and spina bifida.

Kromberg JG, Krause A. Kromberg JG, et al. Among authors: krause a. Am J Med Genet. 1993 Feb 15;45(4):536-7. doi: 10.1002/ajmg.1320450430. Am J Med Genet. 1993. PMID: 8465867 No abstract available.

4

Founder effect and prevalence of myotonic dystrophy in South Africans: molecular studies.

Goldman A, Krause A, Ramsay M, Jenkins T. Goldman A, et al. Among authors: krause a. Am J Hum Genet. 1996 Aug;59(2):445-52. Am J Hum Genet. 1996. PMID: 8755933 Free PMC article.

5

Huntington's disease confirmed by genetic testing in five African families.

Silber E, Kromberg J, Temlett JA, Krause A, Saffer D. Silber E, et al. Among authors: krause a. Mov Disord. 1998 Jul;13(4):726-30. doi: 10.1002/mds.870130420. Mov Disord. 1998. PMID: 9686782

6

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

7

Different molecular basis for spinal muscular atrophy in South African black patients.

Stevens G, Yawitch T, Rodda J, Verhaart S, Krause A. Stevens G, et al. Among authors: krause a. Am J Med Genet. 1999 Oct 29;86(5):420-6. Am J Med Genet. 1999. PMID: 10508982

8

A common Fanconi anemia mutation in black populations of sub-Saharan Africa.

Morgan NV, Essop F, Demuth I, de Ravel T, Jansen S, Tischkowitz M, Lewis CM, Wainwright L, Poole J, Joenje H, Digweed M, Krause A, Mathew CG. Morgan NV, et al. Among authors: krause a. Blood. 2005 May 1;105(9):3542-4. doi: 10.1182/blood-2004-10-3968. Epub 2005 Jan 18. Blood. 2005. PMID: 15657175 Free article.

9

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

10

Roles of genetic counselors in South Africa.

Kromberg JG, Wessels TM, Krause A. Kromberg JG, et al. Among authors: krause a. J Genet Couns. 2013 Dec;22(6):753-61. doi: 10.1007/s10897-013-9606-2. Epub 2013 May 31. J Genet Couns. 2013. PMID: 23723047

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