Bhattacharya SS - Search Results

1

No evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): evidence for genetic heterogeneity.

Inglehearn CF, Jay M, Lester DH, Bashir R, Jay B, Bird AC, Wright AF, Evans HJ, Papiha SS, Bhattacharya SS. Inglehearn CF, et al. Among authors: bhattacharya ss. Genomics. 1990 Jan;6(1):168-73. doi: 10.1016/0888-7543(90)90462-4. Genomics. 1990. PMID: 2303257

2

Autosomal dominant retinitis pigmentosa: four new mutations in rhodopsin, one of them in the retinal attachment site.

Keen TJ, Inglehearn CF, Lester DH, Bashir R, Jay M, Bird AC, Jay B, Bhattacharya SS. Keen TJ, et al. Among authors: bhattacharya ss. Genomics. 1991 Sep;11(1):199-205. doi: 10.1016/0888-7543(91)90119-y. Genomics. 1991. PMID: 1765377

3

Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindred.

Wright AF, Bhattacharya SS, Aldred MA, Jay M, Carothers AD, Thomas NS, Bird AC, Jay B, Evans HJ. Wright AF, et al. Among authors: bhattacharya ss. J Med Genet. 1991 Jul;28(7):453-7. doi: 10.1136/jmg.28.7.453. J Med Genet. 1991. PMID: 1895315 Free PMC article.

4

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.

5

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.

6

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.

7

X-linked retinitis pigmentosa: a molecular genetic approach to isolating the defective genes.

Lindsay S, Jay M, Bower DJ, Adam G, Inglehearn CF, Sealey PG, Papiha SS, Bhattacharya SS. Lindsay S, et al. Among authors: bhattacharya ss. Prog Clin Biol Res. 1989;314:83-97. Prog Clin Biol Res. 1989. PMID: 2692031 Review. No abstract available.

8

Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14.

Wright AF, Bhattacharya SS, Clayton JF, Dempster M, Tippett P, McKeown CM, Jay M, Jay B, Bird AC. Wright AF, et al. Among authors: bhattacharya ss. Am J Hum Genet. 1987 Oct;41(4):635-44. Am J Hum Genet. 1987. PMID: 3477957 Free PMC article.

9

A YAC contig spanning the dominant retinitis pigmentosa locus (RP9) on chromosome 7p.

Keen TJ, Inglehearn CF, Green ED, Cunningham AF, Patel RJ, Peacock RE, Gerken S, White R, Weissenbach J, Bhattacharya SS. Keen TJ, et al. Among authors: bhattacharya ss. Genomics. 1995 Aug 10;28(3):383-8. doi: 10.1006/geno.1995.1165. Genomics. 1995. PMID: 7490071

10

Localization of the aquaporin 1 (AQP1) gene within a YAC contig containing the polymorphic markers D7S632 and D7S526.

Keen TJ, Inglehearn CF, Patel RJ, Green ED, Peluso DC, Bhattacharya SS. Keen TJ, et al. Among authors: bhattacharya ss. Genomics. 1995 Jan 20;25(2):599-600. doi: 10.1016/0888-7543(95)80070-3. Genomics. 1995. PMID: 7540589 No abstract available.

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