Inglehearn CF - Search Results

1

Identification of a locus (LCA9) for Leber's congenital amaurosis on chromosome 1p36.

Keen TJ, Mohamed MD, McKibbin M, Rashid Y, Jafri H, Maumenee IH, Inglehearn CF. Keen TJ, et al. Among authors: inglehearn cf. Eur J Hum Genet. 2003 May;11(5):420-3. doi: 10.1038/sj.ejhg.5200981. Eur J Hum Genet. 2003. PMID: 12734549

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

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.

6

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

7

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

8

A YAC contig spanning the dominant retinitis pigmentosa locus (RP9) on chromosome 7p.

Keen TJ, Inglehearn CF, Green ED, Cunningham AF, Patel RJ, Peacock RE, Gerken S, White R, Weissenbach J, Bhattacharya SS. Keen TJ, et al. Among authors: inglehearn cf. Genomics. 1995 Aug 10;28(3):383-8. doi: 10.1006/geno.1995.1165. Genomics. 1995. PMID: 7490071

9

Localization of the aquaporin 1 (AQP1) gene within a YAC contig containing the polymorphic markers D7S632 and D7S526.

Keen TJ, Inglehearn CF, Patel RJ, Green ED, Peluso DC, Bhattacharya SS. Keen TJ, et al. Among authors: inglehearn cf. Genomics. 1995 Jan 20;25(2):599-600. doi: 10.1016/0888-7543(95)80070-3. Genomics. 1995. PMID: 7540589 No abstract available.

10

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: inglehearn cf. Hum Mol Genet. 1994 Feb;3(2):351-4. doi: 10.1093/hmg/3.2.351. Hum Mol Genet. 1994. PMID: 8004108

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