Hardcastle A - Search Results

1

A 150 bp insertion in the rhodopsin gene of an autosomal dominant retinitis pigmentosa family.

al-Maghtheh M, Kim RY, Hardcastle A, Inglehearn C, Bhattacharya SS. al-Maghtheh M, et al. Among authors: hardcastle a. Hum Mol Genet. 1994 Jan;3(1):205-6. doi: 10.1093/hmg/3.1.205. Hum Mol Genet. 1994. PMID: 8162031 No abstract available.

2

Better fingerprinting with PCR.

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

3

FISH mapping of 22 novel X chromosome cosmids and the isolation of a novel microsatellite on proximal Xp.

Kamakari S, Thiselton D, Lindsay S, Hardcastle A, Bhattacharya S. Kamakari S, et al. Among authors: hardcastle a. Cytogenet Cell Genet. 1995;71(2):151-4. doi: 10.1159/000134096. Cytogenet Cell Genet. 1995. PMID: 7656586

4

Genetic and physical mapping of five novel microsatellite markers on human Xp21.1-p11.22.

Thiselton DL, Lindsay S, Kamakari S, Hardcastle AJ, Roustan P, Bhattacharya SS. Thiselton DL, et al. Among authors: hardcastle aj. Genomics. 1995 Jan 1;25(1):279-81. doi: 10.1016/0888-7543(95)80136-a. Genomics. 1995. PMID: 7774929

5

Rhodopsin mutations in autosomal dominant retinitis pigmentosa.

al-Maghtheh M, Gregory C, Inglehearn C, Hardcastle A, Bhattacharya S. al-Maghtheh M, et al. Among authors: hardcastle a. Hum Mutat. 1993;2(4):249-55. doi: 10.1002/humu.1380020403. Hum Mutat. 1993. PMID: 8401533 Review.

6

cDNA sequence and gene locus of the human retinal phosphoinositide-specific phospholipase-C beta 4 (PLCB4).

Alvarez RA, Ghalayini AJ, Xu P, Hardcastle A, Bhattacharya S, Rao PN, Pettenati MJ, Anderson RE, Baehr W. Alvarez RA, et al. Among authors: hardcastle a. Genomics. 1995 Sep 1;29(1):53-61. doi: 10.1006/geno.1995.1214. Genomics. 1995. PMID: 8530101

7

Nomenclature for inherited diseases of the retina.

Inglehearn CF, Hardcastle AJ. Inglehearn CF, et al. Among authors: hardcastle aj. Am J Hum Genet. 1996 Feb;58(2):433-5. Am J Hum Genet. 1996. PMID: 8571973 Free PMC article. No abstract available.

8

Mapping the RP2 locus for X-linked retinitis pigmentosa on proximal Xp: a genetically defined 5-cM critical region and exclusion of candidate genes by physical mapping.

Thiselton DL, Hampson RM, Nayudu M, Van Maldergem L, Wolf ML, Saha BK, Bhattacharya SS, Hardcastle AJ. Thiselton DL, et al. Among authors: hardcastle aj. Genome Res. 1996 Nov;6(11):1093-102. doi: 10.1101/gr.6.11.1093. Genome Res. 1996. PMID: 8938433 Free article.

9

Genomic organization of the human TIMP-1 gene. Investigation of a causative role in the pathogenesis of X-linked retinitis pigmentosa 2.

Hardcastle AJ, Thiselton DL, Nayudu M, Hampson RM, Bhattacharya SS. Hardcastle AJ, et al. Invest Ophthalmol Vis Sci. 1997 Aug;38(9):1893-6. Invest Ophthalmol Vis Sci. 1997. PMID: 9286280

10

Localization of CSNBX (CSNB4) between the retinitis pigmentosa loci RP2 and RP3 on proximal Xp.

Hardcastle AJ, David-Gray ZK, Jay M, Bird AC, Bhattacharya SS. Hardcastle AJ, et al. Invest Ophthalmol Vis Sci. 1997 Dec;38(13):2750-5. Invest Ophthalmol Vis Sci. 1997. PMID: 9418727

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