Jay M - Search Results

1

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. Among authors: jay b, jay m. 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.

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

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. Among authors: jay m. Hum Mol Genet. 1992 Apr;1(1):41-5. doi: 10.1093/hmg/1.1.41. Hum Mol Genet. 1992. PMID: 1301135

4

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: jay b. 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.

5

Recombination between rhodopsin and locus D3S47 (C17) in rhodopsin retinitis pigmentosa families.

Inglehearn CF, Lester DH, Bashir R, Atif U, Keen TJ, Sertedaki A, Lindsey J, Jay M, Bird AC, Farrar GJ, et al. Inglehearn CF, et al. Among authors: jay m. Am J Hum Genet. 1992 Mar;50(3):590-7. Am J Hum Genet. 1992. PMID: 1539595 Free PMC article.

6

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. Among authors: jay b, jay m. 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.

7

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

8

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: jay m. 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.

9

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: jay b, jay m. Genomics. 1990 Jan;6(1):168-73. doi: 10.1016/0888-7543(90)90462-4. Genomics. 1990. PMID: 2303257

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

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