Bird AC - Search Results

1

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: bird ac. 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.

2

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

3

Linkage refinement localises Sorsby fundus dystrophy between markers D22S275 and D22S278.

Gregory CY, Wijesuriya S, Evans K, Jay M, Bird AC, Bhattacharya SS. Gregory CY, et al. Among authors: bird ac. J Med Genet. 1995 Mar;32(3):240-1. doi: 10.1136/jmg.32.3.240. J Med Genet. 1995. PMID: 7783180 Free PMC article.

4

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: bird ac. Hum Mol Genet. 1994 Feb;3(2):351-4. doi: 10.1093/hmg/3.2.351. Hum Mol Genet. 1994. PMID: 8004108

5

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: bird ac. Am J Hum Genet. 1994 Apr;54(4):675-80. Am J Hum Genet. 1994. PMID: 8128965 Free PMC article.

6

A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p.

Inglehearn CF, Carter SA, Keen TJ, Lindsey J, Stephenson AM, Bashir R, al-Maghtheh M, Moore AT, Jay M, Bird AC, et al. Inglehearn CF, et al. Among authors: bird ac. Nat Genet. 1993 May;4(1):51-3. doi: 10.1038/ng0593-51. Nat Genet. 1993. PMID: 8513323

7

A new family linked to the RP13 locus for autosomal dominant retinitis pigmentosa on distal 17p.

Tarttelin EE, Plant C, Weissenbach J, Bird AC, Bhattacharya SS, Inglehearn CF. Tarttelin EE, et al. Among authors: bird ac. J Med Genet. 1996 Jun;33(6):518-20. doi: 10.1136/jmg.33.6.518. J Med Genet. 1996. PMID: 8782056 Free PMC article.

8

The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16.

Gregory CY, Evans K, Wijesuriya SD, Kermani S, Jay MR, Plant C, Cox N, Bird AC, Bhattacharya SS. Gregory CY, et al. Among authors: bird ac. Hum Mol Genet. 1996 Jul;5(7):1055-9. doi: 10.1093/hmg/5.7.1055. Hum Mol Genet. 1996. PMID: 8817347

9

Localization of CSNBX (CSNB4) between the retinitis pigmentosa loci RP2 and RP3 on proximal Xp.

Hardcastle AJ, David-Gray ZK, Jay M, Bird AC, Bhattacharya SS. Hardcastle AJ, et al. Among authors: bird ac. Invest Ophthalmol Vis Sci. 1997 Dec;38(13):2750-5. Invest Ophthalmol Vis Sci. 1997. PMID: 9418727

10

A linkage survey of 20 dominant retinitis pigmentosa families: frequencies of the nine known loci and evidence for further heterogeneity.

Inglehearn CF, Tarttelin EE, Plant C, Peacock RE, al-Maghtheh M, Vithana E, Bird AC, Bhattacharya SS. Inglehearn CF, et al. Among authors: bird ac. J Med Genet. 1998 Jan;35(1):1-5. doi: 10.1136/jmg.35.1.1. J Med Genet. 1998. PMID: 9475085 Free PMC article.

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