Jay MR - Search Results

1

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: jay mr. Hum Mol Genet. 1996 Jul;5(7):1055-9. doi: 10.1093/hmg/5.7.1055. Hum Mol Genet. 1996. PMID: 8817347

2

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

3

Sorsby's fundus dystrophy in the British Isles: demonstration of a striking founder effect by microsatellite-generated haplotypes.

Wijesuriya SD, Evans K, Jay MR, Davison C, Weber BH, Bird AC, Bhattacharya SS, Gregory CY. Wijesuriya SD, et al. Among authors: jay mr. Genome Res. 1996 Feb;6(2):92-101. doi: 10.1101/gr.6.2.92. Genome Res. 1996. PMID: 8919688 Free article.

4

Assessment of the phenotypic range seen in Doyne honeycomb retinal dystrophy.

Evans K, Gregory CY, Wijesuriya SD, Kermani S, Jay MR, Plant C, Bird AC. Evans K, et al. Among authors: jay mr. Arch Ophthalmol. 1997 Jul;115(7):904-10. doi: 10.1001/archopht.1997.01100160074012. Arch Ophthalmol. 1997. PMID: 9230832

5

The role of molecular genetics in the prenatal diagnosis of retinal dystrophies.

Evans K, Gregory CY, Fryer A, Whittaker J, Duvall-Young J, Bird AC, Jay MR, Bhattacharya SS. Evans K, et al. Among authors: jay mr. Eye (Lond). 1995;9 ( Pt 1):24-8. doi: 10.1038/eye.1995.3. Eye (Lond). 1995. PMID: 7713246

6

A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis pigmentosa.

Inglehearn CF, Keen TJ, Bashir R, Jay M, Fitzke F, Bird AC, Crombie A, Bhattacharya S. Inglehearn CF, et al. Hum Mol Genet. 1992 Apr;1(1):41-5. doi: 10.1093/hmg/1.1.41. Hum Mol Genet. 1992. PMID: 1301135

7

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. 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.

8

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. Am J Hum Genet. 1991 Jan;48(1):26-30. Am J Hum Genet. 1991. PMID: 1985460 Free PMC article.

9

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

10

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. 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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

84 results

Search Page

Filters