Lester DH - Search Results

1

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: lester dh. Am J Hum Genet. 1992 Mar;50(3):590-7. Am J Hum Genet. 1992. PMID: 1539595 Free PMC article.

2

Autosomal dominant retinitis pigmentosa: four new mutations in rhodopsin, one of them in the retinal attachment site.

Keen TJ, Inglehearn CF, Lester DH, Bashir R, Jay M, Bird AC, Jay B, Bhattacharya SS. Keen TJ, et al. Among authors: lester dh. Genomics. 1991 Sep;11(1):199-205. doi: 10.1016/0888-7543(91)90119-y. Genomics. 1991. PMID: 1765377

3

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

4

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: lester dh. Genomics. 1990 Jan;6(1):168-73. doi: 10.1016/0888-7543(90)90462-4. Genomics. 1990. PMID: 2303257

5

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.

6

Retinitis pigmentosa and mutations in rhodopsin.

Bhattacharya S, Lester D, Keen J, Bashir R, Lauffart B, Inglehearn CF, Jay M, Bird AC. Bhattacharya S, et al. Lancet. 1991 Jan 19;337(8734):185. doi: 10.1016/0140-6736(91)90858-m. Lancet. 1991. PMID: 1670831 No abstract available.

7

Rapid detection of single base mismatches as heteroduplexes on Hydrolink gels.

Keen J, Lester D, Inglehearn C, Curtis A, Bhattacharya S. Keen J, et al. Trends Genet. 1991 Jan;7(1):5. doi: 10.1016/0168-9525(91)90004-a. Trends Genet. 1991. PMID: 2003336 No abstract available.

8

Better fingerprinting with PCR.

Bellamy R, Inglehearn C, Lester D, Hardcastle A, Bhattacharya S. Bellamy R, et al. Trends Genet. 1990 Feb;6(2):32. doi: 10.1016/0168-9525(90)90054-a. Trends Genet. 1990. PMID: 2336717 No abstract available.

9

Linkage analysis in X-linked congenital stationary night blindness.

Aldred MA, Dry KL, Sharp DM, Van Dorp DB, Brown J, Hardwick LJ, Lester DH, Pryde FE, Teague PW, Jay M, et al. Aldred MA, et al. Among authors: lester dh. Genomics. 1992 Sep;14(1):99-104. doi: 10.1016/s0888-7543(05)80289-7. Genomics. 1992. PMID: 1427834

10

Genetic analysis of a kindred with X-linked mental handicap and retinitis pigmentosa.

Aldred MA, Dry KL, Knight-Jones EB, Hardwick LJ, Teague PW, Lester DH, Brown J, Spowart G, Carothers AD, Raeburn JA, et al. Aldred MA, et al. Among authors: lester dh. Am J Hum Genet. 1994 Nov;55(5):916-22. Am J Hum Genet. 1994. PMID: 7977353 Free PMC article.

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