Ramesar R - Search Results

1

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

2

Digitotalar dysmorphism: Molecular elucidation.

Vorster AA, Beighton P, Ramesar RS. Vorster AA, et al. S Afr Med J. 2016 Feb 2;106(3):253-5. doi: 10.7196/SAMJ.2016.v106i3.10134. S Afr Med J. 2016. PMID: 26915936

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. 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

4

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: ramesar r. Hum Mol Genet. 1995 Aug;4(8):1459-62. doi: 10.1093/hmg/4.8.1459. Hum Mol Genet. 1995. PMID: 7581389

5

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

6

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

7

Retinitis pigmentosa in southern Africa.

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

8

Mseleni joint disease--a molecular genetic approach to defining the aetiology.

Ballo R, Viljoen D, Machado M, Keene D, Horton W, Fredlund V, Jacobs M, Martell R, Beighton P, Ramesar R. Ballo R, et al. Among authors: ramesar r. S Afr Med J. 1996 Aug;86(8):956-8. S Afr Med J. 1996. PMID: 8823421

9

Retinitis pigmentosa locus on 17q (RP17): fine localization to 17q22 and exclusion of the PDEG and TIMP2 genes.

Bardien S, Ramesar R, Bhattacharya S, Greenberg J. Bardien S, et al. Among authors: ramesar r. Hum Genet. 1997 Nov;101(1):13-7. doi: 10.1007/s004390050577. Hum Genet. 1997. PMID: 9385361

10

A photoreceptor gene mutation in an indigenous black African family with retinitis pigmentosa identified using a rapid screening approach for common rhodopsin mutations.

Greenberg J, Franz T, Goliath R, Ramesar R. Greenberg J, et al. Among authors: ramesar r. S Afr Med J. 1999 Aug;89(8):877-8. S Afr Med J. 1999. PMID: 10488366

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