Wright AF - Search Results

1

A genetic linkage study of a kindred with X-linked retinitis pigmentosa.

Bhattacharya SS, Clayton JF, Harper PS, Hoare GW, Jay MR, Lyness AL, Wright AF. Bhattacharya SS, et al. Among authors: wright af. Br J Ophthalmol. 1985 May;69(5):340-7. doi: 10.1136/bjo.69.5.340. Br J Ophthalmol. 1985. PMID: 3994951 Free PMC article.

2

Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa.

Coleman M, Bhattacharya S, Lindsay S, Wright A, Jay M, Litt M, Craig I, Davies K. Coleman M, et al. Am J Hum Genet. 1990 Dec;47(6):935-40. Am J Hum Genet. 1990. PMID: 2239970 Free PMC article.

3

Difference between RP2 and RP3 phenotypes in X linked retinitis pigmentosa.

Flaxel CJ, Jay M, Thiselton DL, Nayudu M, Hardcastle AJ, Wright A, Bird AC. Flaxel CJ, et al. Br J Ophthalmol. 1999 Oct;83(10):1144-8. doi: 10.1136/bjo.83.10.1144. Br J Ophthalmol. 1999. PMID: 10502575 Free PMC article.

4

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. 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.

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: wright af. 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

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: wright af. Genomics. 1990 Jan;6(1):168-73. doi: 10.1016/0888-7543(90)90462-4. Genomics. 1990. PMID: 2303257

7

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: wright af. Am J Hum Genet. 1990 Sep;47(3):536-41. Am J Hum Genet. 1990. PMID: 2393026 Free PMC article.

8

Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 (L1.28): further linkage data, heterogeneity testing, and risk estimation.

Clayton JF, Wright AF, Jay M, McKeown CM, Dempster M, Jay BS, Bird AC, Bhattacharya SS. Clayton JF, et al. Among authors: wright af. Hum Genet. 1986 Oct;74(2):168-71. doi: 10.1007/BF00282083. Hum Genet. 1986. PMID: 2876947

9

A genetic linkage study of choroideremia.

Jay M, Wright AF, Clayton JF, Deans M, Dempster M, Bhattacharya SS, Jay B. Jay M, et al. Among authors: wright af. Ophthalmic Paediatr Genet. 1986 Dec;7(3):201-4. doi: 10.3109/13816818609004139. Ophthalmic Paediatr Genet. 1986. PMID: 2882457

10

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. Am J Hum Genet. 1987 Oct;41(4):635-44. Am J Hum Genet. 1987. PMID: 3477957 Free PMC article.

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