Ramsay M - Search Results

1

Biology and genetics of oculocutaneous albinism and vitiligo - common pigmentation disorders in southern Africa.

Manga P, Kerr R, Ramsay M, Kromberg JG. Manga P, et al. Among authors: ramsay m. S Afr Med J. 2013 Jul 29;103(12 Suppl 1):984-8. doi: 10.7196/samj.7046. S Afr Med J. 2013. PMID: 24300644

2

Professor Trefor Jenkins: a tribute.

Kromberg JG, Ramsay M, Krause A, Soodyall H. Kromberg JG, et al. Among authors: ramsay m. S Afr Med J. 2013 Oct 16;103(12 Suppl 1):956-1034. doi: 10.7196/samj.7627. S Afr Med J. 2013. PMID: 24300658 No abstract available.

3

Rufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 gene.

Manga P, Kromberg JG, Box NF, Sturm RA, Jenkins T, Ramsay M. Manga P, et al. Among authors: ramsay m. Am J Hum Genet. 1997 Nov;61(5):1095-101. doi: 10.1086/301603. Am J Hum Genet. 1997. PMID: 9345097 Free PMC article.

4

In Southern Africa, brown oculocutaneous albinism (BOCA) maps to the OCA2 locus on chromosome 15q: P-gene mutations identified.

Manga P, Kromberg J, Turner A, Jenkins T, Ramsay M. Manga P, et al. Among authors: ramsay m. Am J Hum Genet. 2001 Mar;68(3):782-7. doi: 10.1086/318800. Epub 2001 Feb 9. Am J Hum Genet. 2001. PMID: 11179026 Free PMC article.

5

Identification of P gene mutations in individuals with oculocutaneous albinism in sub-Saharan Africa.

Kerr R, Stevens G, Manga P, Salm S, John P, Haw T, Ramsay M. Kerr R, et al. Among authors: ramsay m. Hum Mutat. 2000;15(2):166-72. doi: 10.1002/(SICI)1098-1004(200002)15:2<166::AID-HUMU5>3.0.CO;2-Z. Hum Mutat. 2000. PMID: 10649493

6

In quest of the tyrosinase-positive oculocutaneous albinism gene.

Jenkins T, Heim RA, Dunn DS, Zwane E, Colman MA, Ramsay M, Kromberg JG. Jenkins T, et al. Among authors: ramsay m. Ophthalmic Paediatr Genet. 1990 Dec;11(4):251-4. doi: 10.3109/13816819009015710. Ophthalmic Paediatr Genet. 1990. PMID: 1982896

7

The tyrosinase-positive oculocutaneous albinism gene shows locus homogeneity on chromosome 15q11-q13 and evidence of multiple mutations in southern African negroids.

Kedda MA, Stevens G, Manga P, Viljoen C, Jenkins T, Ramsay M. Kedda MA, et al. Among authors: ramsay m. Am J Hum Genet. 1994 Jun;54(6):1078-84. Am J Hum Genet. 1994. PMID: 8198130 Free PMC article.

8

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.

9

Oculocutaneous albinism (OCA2) in sub-Saharan Africa: distribution of the common 2.7-kb P gene deletion mutation.

Stevens G, Ramsay M, Jenkins T. Stevens G, et al. Among authors: ramsay m. Hum Genet. 1997 Apr;99(4):523-7. doi: 10.1007/s004390050400. Hum Genet. 1997. PMID: 9099845

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,241 results

Search Page

Filters