Goldman A - Search Results

1

Evidence that a dodecamer duplication in the gene HOPA in Xq13 is not associated with mental retardation.

Friez MJ, Essop FB, Krause A, Castiglia L, Ragusa A, Sossey-Alaoui K, Nelson RL, May MM, Michaelis RC, Srivastava AK, Schwartz CE, Stevenson RE, Goldman A, Villard L, Longshore JW. Friez MJ, et al. Among authors: goldman a. Hum Genet. 2000 Jan;106(1):36-9. doi: 10.1007/s004390051006. Hum Genet. 2000. PMID: 10982179

2

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: goldman a. Am J Hum Genet. 1996 Jun;58(6):1303-8. Am J Hum Genet. 1996. PMID: 8651308 Free PMC article.

3

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

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

4

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

Goldman A, Jenkins T, Krause A. Goldman A, et al. 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.

5

Fragile X syndrome occurs in the South African black population.

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

6

Ethnicity and myotonic dystrophy: a possible explanation for its absence in sub-Saharan Africa.

Goldman A, Ramsay M, Jenkins T. Goldman A, et al. Ann Hum Genet. 1996 Jan;60(1):57-65. doi: 10.1111/j.1469-1809.1996.tb01172.x. Ann Hum Genet. 1996. PMID: 8835099

7

New founder haplotypes at the myotonic dystrophy locus in southern Africa.

Goldman A, Ramsay M, Jenkins T. Goldman A, et al. Am J Hum Genet. 1995 Jun;56(6):1373-8. Am J Hum Genet. 1995. PMID: 7762560 Free PMC article.

8

The molecular basis of cystic fibrosis in South Africa.

Goldman A, Labrum R, Claustres M, Desgeorges M, Guittard C, Wallace A, Ramsay M. Goldman A, et al. Clin Genet. 2001 Jan;59(1):37-41. doi: 10.1034/j.1399-0004.2001.590106.x. Clin Genet. 2001. PMID: 11168023

9

Analysis of 40 known cystic fibrosis mutations in South African patients.

Goldman A, Jenkins T, Ramsay M. Goldman A, et al. Clin Genet. 1994 Dec;46(6):398-400. doi: 10.1111/j.1399-0004.1994.tb04405.x. Clin Genet. 1994. PMID: 7889655

10

A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy mutations.

Tishkoff SA, Goldman A, Calafell F, Speed WC, Deinard AS, Bonne-Tamir B, Kidd JR, Pakstis AJ, Jenkins T, Kidd KK. Tishkoff SA, et al. Among authors: goldman a. Am J Hum Genet. 1998 Jun;62(6):1389-402. doi: 10.1086/301861. Am J Hum Genet. 1998. PMID: 9585589 Free PMC article.

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