Ramsay M - Search Results

1

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

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

2

Glucose-6-phosphate dehydrogenase (G6PD) electrophoretic variants and the PvuII polymorphism in southern African populations.

Coetzee MJ, Bartleet SC, Ramsay M, Jenkins T. Coetzee MJ, et al. Among authors: ramsay m. Hum Genet. 1992 Apr;89(1):111-3. doi: 10.1007/BF00207056. Hum Genet. 1992. PMID: 1349560

3

The tyrosinase-positive oculocutaneous albinism locus maps to chromosome 15q11.2-q12.

Ramsay M, Colman MA, Stevens G, Zwane E, Kromberg J, Farrall M, Jenkins T. Ramsay M, et al. Am J Hum Genet. 1992 Oct;51(4):879-84. Am J Hum Genet. 1992. PMID: 1415228 Free PMC article.

4

The Y-associated XY275 low allele is not restricted to indigenous African peoples.

Spurdle A, Ramsay M, Jenkins T. Spurdle A, et al. Among authors: ramsay m. Am J Hum Genet. 1992 Jun;50(6):1301-7. Am J Hum Genet. 1992. PMID: 1598910 Free PMC article.

5

Globin gene-associated restriction-fragment-length polymorphisms in southern African peoples.

Ramsay M, Jenkins T. Ramsay M, et al. Am J Hum Genet. 1987 Dec;41(6):1132-44. Am J Hum Genet. 1987. PMID: 2891298 Free PMC article.

6

Alpha-globin gene cluster haplotypes in the Kalahari San and southern African Bantu-speaking blacks.

Ramsay M, Jenkins T. Ramsay M, et al. Am J Hum Genet. 1988 Oct;43(4):527-33. Am J Hum Genet. 1988. PMID: 2902790 Free PMC article.

7

Mutations for the autosomal recessive and autosomal dominant forms of polycystic kidney disease are not allelic.

Ramsay M, Reeders ST, Thomson PD, Milner LS, Lazarou L, Barratt TM, Yau A, Lehmann OJ, Jenkins T. Ramsay M, et al. Hum Genet. 1988 May;79(1):73-5. doi: 10.1007/BF00291714. Hum Genet. 1988. PMID: 3163321

8

XX true hermaphroditism in southern African blacks: an enigma of primary sexual differentiation.

Ramsay M, Bernstein R, Zwane E, Page DC, Jenkins T. Ramsay M, et al. Am J Hum Genet. 1988 Jul;43(1):4-13. Am J Hum Genet. 1988. PMID: 3163890 Free PMC article.

9

An intragenic deletion of the P gene is the common mutation causing tyrosinase-positive oculocutaneous albinism in southern African Negroids.

Stevens G, van Beukering J, Jenkins T, Ramsay M. Stevens G, et al. Among authors: ramsay m. Am J Hum Genet. 1995 Mar;56(3):586-91. Am J Hum Genet. 1995. PMID: 7887411 Free PMC article.

10

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

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

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