Krause A - Search Results

1

Feasibility of prenatal diagnosis and carrier detection in South African haemophilia A patients.

Dangerfield BT, Manga P, Field SP, Hartman E, Jenkins T, Krause A. Dangerfield BT, et al. Among authors: krause a. Br J Haematol. 1997 Jun;97(3):558-60. doi: 10.1046/j.1365-2141.1997.892905.x. Br J Haematol. 1997. PMID: 9207400 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

Pseudocholinesterase variation in southern African populations.

Krause A, Lane AB, Jenkins T. Krause A, et al. S Afr Med J. 1987 Mar 7;71(5):298-301. S Afr Med J. 1987. PMID: 3563754

4

The high frequency of the Hb B2 variant in the Herero population: a founder effect?

Spurdle AB, Krause A, Ramsay M, Jenkins T. Spurdle AB, et al. Among authors: krause a. Hemoglobin. 1994 Sep;18(4-5):317-23. doi: 10.3109/03630269408996197. Hemoglobin. 1994. PMID: 7852086

5

Beta-globin haplotype analysis suggests that a major source of Malagasy ancestry is derived from Bantu-speaking Negroids.

Hewitt R, Krause A, Goldman A, Campbell G, Jenkins T. Hewitt R, et al. Among authors: krause a. Am J Hum Genet. 1996 Jun;58(6):1303-8. Am J Hum Genet. 1996. PMID: 8651308 Free PMC article.

6

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.

7

Screening for Alzheimer's disease.

Krause A, Jenkins T. Krause A, et al. S Afr Med J. 1997 Feb;87(2):128-30. S Afr Med J. 1997. PMID: 9107213 No abstract available.

8

Fragile X syndrome occurs in the South African black population.

Goldman A, Krause A, Jenkins T. Goldman A, et al. Among authors: krause a. S Afr Med J. 1997 Apr;87(4):418-20. S Afr Med J. 1997. PMID: 9254780 No abstract available.

9

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

10

Molecular evidence that fragile X syndrome occurs in the South African black population.

Goldman A, Jenkins T, Krause A. Goldman A, et al. Among authors: krause a. J Med Genet. 1998 Oct;35(10):878. doi: 10.1136/jmg.35.10.878. J Med Genet. 1998. PMID: 9783718 Free PMC article. No abstract available.

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