Greenberg J - Search Results

1

Hearing impairment and pigmentary disturbance.

Beighton P, Ramesar R, Winship I, Viljoen D, Greenberg J, Young K, Curtis D, Sellars S. Beighton P, et al. Among authors: greenberg j. Ann N Y Acad Sci. 1991;630:152-66. doi: 10.1111/j.1749-6632.1991.tb19584.x. Ann N Y Acad Sci. 1991. PMID: 1952586 Review.

2

Mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene account for a continuous range of phenotypes in human piebaldism.

Spritz RA, Holmes SA, Ramesar R, Greenberg J, Curtis D, Beighton P. Spritz RA, et al. Among authors: greenberg j. Am J Hum Genet. 1992 Nov;51(5):1058-65. Am J Hum Genet. 1992. PMID: 1384325 Free PMC article.

3

Retinitis pigmentosa, AD type I: exclusion of linkage to D3S47 (C17) in a large South African family of British origin.

Greenberg J, Babaya M, Ramesar R, Beighton P. Greenberg J, et al. Clin Genet. 1992 Jun;41(6):322-5. doi: 10.1111/j.1399-0004.1992.tb03406.x. Clin Genet. 1992. PMID: 1623630

4

Genetic mapping of retinitis pigmentosa--implications for South African patients.

Greenberg J, Ramesar R, Beighton P. Greenberg J, et al. S Afr Med J. 1994 Jul;84(7):410-2. S Afr Med J. 1994. PMID: 7709305

5

A new locus for autosomal dominant retinitis pigmentosa on the short arm of chromosome 17.

Greenberg J, Goliath R, Beighton P, Ramesar R. Greenberg J, et al. Hum Mol Genet. 1994 Jun;3(6):915-8. doi: 10.1093/hmg/3.6.915. Hum Mol Genet. 1994. PMID: 7951236

6

A splice junction mutation in PAX3 causes Waardenburg syndrome in a South African family.

Butt J, Greenberg J, Winship I, Sellars S, Beighton P, Ramesar R. Butt J, et al. Among authors: greenberg j. Hum Mol Genet. 1994 Jan;3(1):197-8. doi: 10.1093/hmg/3.1.197. Hum Mol Genet. 1994. PMID: 8162027 No abstract available.

7

Retinitis pigmentosa in southern Africa.

Greenberg J, Bartmann L, Ramesar R, Beighton P. Greenberg J, et al. Clin Genet. 1993 Nov;44(5):232-5. doi: 10.1111/j.1399-0004.1993.tb03888.x. Clin Genet. 1993. PMID: 8313621

8

Mapping of the gene for cleidocranial dysplasia in the historical Cape Town (Arnold) kindred and evidence for locus homogeneity.

Ramesar RS, Greenberg J, Martin R, Goliath R, Bardien S, Mundlos S, Beighton P. Ramesar RS, et al. Among authors: greenberg j. J Med Genet. 1996 Jun;33(6):511-4. doi: 10.1136/jmg.33.6.511. J Med Genet. 1996. PMID: 8782054 Free PMC article.

9

Familial streptomycin ototoxicity in a South African family: a mitochondrial disorder.

Gardner JC, Goliath R, Viljoen D, Sellars S, Cortopassi G, Hutchin T, Greenberg J, Beighton P. Gardner JC, et al. Among authors: greenberg j. J Med Genet. 1997 Nov;34(11):904-6. doi: 10.1136/jmg.34.11.904. J Med Genet. 1997. PMID: 9391883 Free PMC article.

10

An eighth locus for autosomal dominant retinitis pigmentosa is linked to chromosome 17q.

Bardien S, Ebenezer N, Greenberg J, Inglehearn CF, Bartmann L, Goliath R, Beighton P, Ramesar R, Bhattacharya SS. Bardien S, et al. Among authors: greenberg j. Hum Mol Genet. 1995 Aug;4(8):1459-62. doi: 10.1093/hmg/4.8.1459. Hum Mol Genet. 1995. PMID: 7581389

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