Wright A - Search Results

1

Deletions in patients with classical choroideremia vary in size from 45 kb to several megabases.

Cremers FP, Sankila EM, Brunsmann F, Jay M, Jay B, Wright A, Pinckers AJ, Schwartz M, van de Pol DJ, Wieringa B, et al. Cremers FP, et al. Among authors: wright a. Am J Hum Genet. 1990 Oct;47(4):622-8. Am J Hum Genet. 1990. PMID: 2220804 Free PMC article.

2

Linkage studies and deletion screening in choroideremia.

Wright AF, Nussbaum RL, Bhattacharya SS, Jay M, Lesko JG, Evans HJ, Jay B. Wright AF, et al. J Med Genet. 1990 Aug;27(8):496-8. doi: 10.1136/jmg.27.8.496. J Med Genet. 1990. PMID: 1976814 Free PMC article.

3

DXS26 (HU16) is located in Xq21.1.

Sankila EM, Bruns GA, Schwartz M, Nikoskelainen E, Niebuhr E, Hodgson SV, Wright AF, de la Chapelle A. Sankila EM, et al. Among authors: wright af. Hum Genet. 1990 Jun;85(1):117-20. doi: 10.1007/BF00276335. Hum Genet. 1990. PMID: 2162804

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

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

7

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.

8

Retinitis pigmentosa families showing apparent X linked inheritance but unlinked to the RP2 or RP3 loci.

Aldred MA, Teague PW, Jay M, Bundey S, Redmond RM, Jay B, Bird AC, Bhattacharya SS, Wright AF. Aldred MA, et al. Among authors: wright af. J Med Genet. 1994 Nov;31(11):848-52. doi: 10.1136/jmg.31.11.848. J Med Genet. 1994. PMID: 7853368 Free PMC article.

9

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. Among authors: wright a. Am J Hum Genet. 1990 Dec;47(6):935-40. Am J Hum Genet. 1990. PMID: 2239970 Free PMC article.

10

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.

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