Bird AC - Search Results

1

Nine generations of a family with autosomal dominant retinitis pigmentosa and evidence of variable expressivity from census records.

Jay M, Bird AC, Moore AN, Jay B. Jay M, et al. Among authors: bird ac. J Med Genet. 1992 Dec;29(12):906-10. doi: 10.1136/jmg.29.12.906. J Med Genet. 1992. PMID: 1479605 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

Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19q.

Evans K, al-Maghtheh M, Fitzke FW, Moore AT, Jay M, Inglehearn CF, Arden GB, Bird AC. Evans K, et al. Among authors: bird ac. Br J Ophthalmol. 1995 Sep;79(9):841-6. doi: 10.1136/bjo.79.9.841. Br J Ophthalmol. 1995. PMID: 7488604 Free PMC article.

4

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.

5

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.

6

Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expression.

Kim RY, Fitzke FW, Moore AT, Jay M, Inglehearn C, Arden GB, Bhattacharya SS, Bird AC. Kim RY, et al. Among authors: bird ac. Br J Ophthalmol. 1995 Jan;79(1):23-7. doi: 10.1136/bjo.79.1.23. Br J Ophthalmol. 1995. PMID: 7880785 Free PMC article.

7

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

8

Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic study.

Moore AT, Fitzke F, Jay M, Arden GB, Inglehearn CF, Keen TJ, Bhattacharya SS, Bird AC. Moore AT, et al. Among authors: bird ac. Br J Ophthalmol. 1993 Aug;77(8):473-9. doi: 10.1136/bjo.77.8.473. Br J Ophthalmol. 1993. PMID: 8025041 Free PMC article.

9

Ocular manifestations in autosomal dominant retinitis pigmentosa with a Lys-296-Glu rhodopsin mutation at the retinal binding site.

Owens SL, Fitzke FW, Inglehearn CF, Jay M, Keen TJ, Arden GB, Bhattacharya SS, Bird AC. Owens SL, et al. Among authors: bird ac. Br J Ophthalmol. 1994 May;78(5):353-8. doi: 10.1136/bjo.78.5.353. Br J Ophthalmol. 1994. PMID: 8025068 Free PMC article.

10

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.

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