Inglehearn CF - Search Results

1

Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa.

Chakarova CF, Hims MM, Bolz H, Abu-Safieh L, Patel RJ, Papaioannou MG, Inglehearn CF, Keen TJ, Willis C, Moore AT, Rosenberg T, Webster AR, Bird AC, Gal A, Hunt D, Vithana EN, Bhattacharya SS. Chakarova CF, et al. Among authors: inglehearn cf. Hum Mol Genet. 2002 Jan 1;11(1):87-92. doi: 10.1093/hmg/11.1.87. Hum Mol Genet. 2002. PMID: 11773002

2

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

3

Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutation.

Moore AT, Fitzke FW, Kemp CM, Arden GB, Keen TJ, Inglehearn CF, Bhattacharya SS, Bird AC. Moore AT, et al. Among authors: inglehearn cf. Br J Ophthalmol. 1992 Aug;76(8):465-9. doi: 10.1136/bjo.76.8.465. Br J Ophthalmol. 1992. PMID: 1390527 Free PMC article.

4

Exclusion of chromosome 6 and 8 locations in nonrhodopsin autosomal dominant retinitis pigmentosa families: further locus heterogeneity in adRP.

Bashir R, Inglehearn CF, Keen TJ, Lindsey J, Atif U, Carter SA, Stephenson AM, Jackson A, Jay M, Bird AC, et al. Bashir R, et al. Among authors: inglehearn cf. Genomics. 1992 Sep;14(1):191-3. doi: 10.1016/s0888-7543(05)80306-4. Genomics. 1992. PMID: 1427827

5

Molecular genetics of inherited retinal degenerations.

Lindsay S, Inglehearn CF, Curtis A, Bhattacharya S. Lindsay S, et al. Among authors: inglehearn cf. Curr Opin Genet Dev. 1992 Jun;2(3):459-66. doi: 10.1016/s0959-437x(05)80158-3. Curr Opin Genet Dev. 1992. PMID: 1504622 Review.

6

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

7

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. Among authors: inglehearn cf. Lancet. 1991 Jan 19;337(8734):185. doi: 10.1016/0140-6736(91)90858-m. Lancet. 1991. PMID: 1670831 No abstract available.

8

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: inglehearn cf. Genomics. 1991 Sep;11(1):199-205. doi: 10.1016/0888-7543(91)90119-y. Genomics. 1991. PMID: 1765377

9

Increased band sharing in DNA fingerprints of an inbred human population.

Bellamy RJ, Inglehearn CF, Jalili IK, Jeffreys AJ, Bhattacharya SS. Bellamy RJ, et al. Among authors: inglehearn cf. Hum Genet. 1991 Jul;87(3):341-7. doi: 10.1007/BF00200917. Hum Genet. 1991. PMID: 1864611

10

New strategies in molecular genetic studies of X-linked retinitis pigmentosa.

Jay M, Inglehearn C. Jay M, et al. Eye (Lond). 1990;4 ( Pt 5):737-42. doi: 10.1038/eye.1990.105. Eye (Lond). 1990. PMID: 1980893

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