Ramesar R - 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: ramesar r. 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

Piebaldism: an autonomous autosomal dominant entity.

Winship I, Young K, Martell R, Ramesar R, Curtis D, Beighton P. Winship I, et al. Among authors: ramesar r. Clin Genet. 1991 May;39(5):330-7. doi: 10.1111/j.1399-0004.1991.tb03039.x. Clin Genet. 1991. PMID: 1860249

3

Spondyloepiphyseal dysplasia in a Cape Town family: linkage with the gene for type II collagen (COL2A1).

Ramesar R, Beighton P. Ramesar R, et al. Am J Med Genet. 1992 Jul 15;43(5):833-8. doi: 10.1002/ajmg.1320430516. Am J Med Genet. 1992. PMID: 1353665

4

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: ramesar r. Am J Hum Genet. 1992 Nov;51(5):1058-65. Am J Hum Genet. 1992. PMID: 1384325 Free PMC article.

5

Evidence for paternal imprinting in familial Beckwith-Wiedemann syndrome.

Viljoen D, Ramesar R. Viljoen D, et al. Among authors: ramesar r. J Med Genet. 1992 Apr;29(4):221-5. doi: 10.1136/jmg.29.4.221. J Med Genet. 1992. PMID: 1583639 Free PMC article.

6

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. Among authors: ramesar r. Clin Genet. 1992 Jun;41(6):322-5. doi: 10.1111/j.1399-0004.1992.tb03406.x. Clin Genet. 1992. PMID: 1623630

7

Beals syndrome: clinical and molecular investigations in a kindred of Indian descent.

Viljoen D, Ramesar R, Behari D. Viljoen D, et al. Among authors: ramesar r. Clin Genet. 1991 Mar;39(3):181-8. doi: 10.1111/j.1399-0004.1991.tb03009.x. Clin Genet. 1991. PMID: 1674682

8

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

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

9

Autosomal dominant (Beukes) premature degenerative osteoarthropathy of the hip joint unlinked to COL2A1.

Beighton P, Cilliers HJ, Ramesar R. Beighton P, et al. Among authors: ramesar r. Am J Med Genet. 1994 Dec 1;53(4):348-51. doi: 10.1002/ajmg.1320530408. Am J Med Genet. 1994. PMID: 7864044

10

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. Among authors: ramesar r. Hum Mol Genet. 1994 Jun;3(6):915-8. doi: 10.1093/hmg/3.6.915. Hum Mol Genet. 1994. PMID: 7951236

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