Bhattacharya SS - Search Results

1

Increased band sharing in DNA fingerprints of an inbred human population.

Bellamy RJ, Inglehearn CF, Jalili IK, Jeffreys AJ, Bhattacharya SS. Bellamy RJ, et al. Among authors: bhattacharya ss. Hum Genet. 1991 Jul;87(3):341-7. doi: 10.1007/BF00200917. Hum Genet. 1991. PMID: 1864611

2

A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa.

Inglehearn CF, Bashir R, Lester DH, Jay M, Bird AC, Bhattacharya SS. Inglehearn CF, et al. Among authors: bhattacharya ss. Am J Hum Genet. 1991 Jan;48(1):26-30. Am J Hum Genet. 1991. PMID: 1985460 Free PMC article.

3

Linkage of internal minisatellite loci on chromosome 1 and exclusion of autosomal dominant retinitis pigmentosa proximal to rhesus.

Inglehearn CF, Papiha SS, Jay M, Wright AF, Moore AT, Bhattacharya SS. Inglehearn CF, et al. Among authors: bhattacharya ss. J Med Genet. 1990 Jan;27(1):14-6. doi: 10.1136/jmg.27.1.14. J Med Genet. 1990. PMID: 2106582 Free PMC article.

4

Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another: confirmation of genetic heterogeneity.

Lester DH, Inglehearn CF, Bashir R, Ackford H, Esakowitz L, Jay M, Bird AC, Wright AF, Papiha SS, Bhattacharya SS. Lester DH, et al. Among authors: bhattacharya ss. Am J Hum Genet. 1990 Sep;47(3):536-41. Am J Hum Genet. 1990. PMID: 2393026 Free PMC article.

5

A 150 bp insertion in the rhodopsin gene of an autosomal dominant retinitis pigmentosa family.

al-Maghtheh M, Kim RY, Hardcastle A, Inglehearn C, Bhattacharya SS. al-Maghtheh M, et al. Among authors: bhattacharya ss. Hum Mol Genet. 1994 Jan;3(1):205-6. doi: 10.1093/hmg/3.1.205. Hum Mol Genet. 1994. PMID: 8162031 No abstract available.

6

Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa.

Chakarova CF, Hims MM, Bolz H, Abu-Safieh L, Patel RJ, Papaioannou MG, Inglehearn CF, Keen TJ, Willis C, Moore AT, Rosenberg T, Webster AR, Bird AC, Gal A, Hunt D, Vithana EN, Bhattacharya SS. Chakarova CF, et al. Among authors: bhattacharya ss. Hum Mol Genet. 2002 Jan 1;11(1):87-92. doi: 10.1093/hmg/11.1.87. Hum Mol Genet. 2002. PMID: 11773002

7

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

8

Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19.

al-Maghtheh M, Inglehearn CF, Keen TJ, Evans K, Moore AT, Jay M, Bird AC, Bhattacharya SS. al-Maghtheh M, et al. Among authors: bhattacharya ss. Hum Mol Genet. 1994 Feb;3(2):351-4. doi: 10.1093/hmg/3.2.351. Hum Mol Genet. 1994. PMID: 8004108

9

Further refinement of the location for autosomal dominant retinitis pigmentosa on chromosome 7p (RP9).

Inglehearn CF, Keen TJ, al-Maghtheh M, Gregory CY, Jay MR, Moore AT, Bird AC, Bhattacharya SS. Inglehearn CF, et al. Among authors: bhattacharya ss. Am J Hum Genet. 1994 Apr;54(4):675-80. Am J Hum Genet. 1994. PMID: 8128965 Free PMC article.

10

Linkage of congenital hereditary endothelial dystrophy to chromosome 20.

Toma NM, Ebenezer ND, Inglehearn CF, Plant C, Ficker LA, Bhattacharya SS. Toma NM, et al. Among authors: bhattacharya ss. Hum Mol Genet. 1995 Dec;4(12):2395-8. doi: 10.1093/hmg/4.12.2395. Hum Mol Genet. 1995. PMID: 8634716

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