Hardwick LJ - Search Results

1

Identification of a novel gene, ETX1 from Xp21.1, a candidate gene for X-linked retintis pigmentosa (RP3).

Dry KL, Aldred MA, Edgar AJ, Brown J, Manson FD, Ho MF, Prosser J, Hardwick LJ, Lennon AA, Thomson K, et al. Dry KL, et al. Among authors: hardwick lj. Hum Mol Genet. 1995 Dec;4(12):2347-53. doi: 10.1093/hmg/4.12.2347. Hum Mol Genet. 1995. PMID: 8634709

2

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: hardwick lj. Am J Hum Genet. 1994 Nov;55(5):916-22. Am J Hum Genet. 1994. PMID: 7977353 Free PMC article.

3

Heterogeneity analysis in 40 X-linked retinitis pigmentosa families.

Teague PW, Aldred MA, Jay M, Dempster M, Harrison C, Carothers AD, Hardwick LJ, Evans HJ, Strain L, Brock DJ, et al. Teague PW, et al. Among authors: hardwick lj. Am J Hum Genet. 1994 Jul;55(1):105-11. Am J Hum Genet. 1994. PMID: 8023838 Free PMC article.

4

An STR polymorphism at the CYBB locus.

Hardwick LJ, Brown J, Wright AF. Hardwick LJ, et al. Hum Mol Genet. 1993 Oct;2(10):1755. doi: 10.1093/hmg/2.10.1755. Hum Mol Genet. 1993. PMID: 8268956 No abstract available.

5

Linkage analysis in a family with complete type congenital stationary night blindness with and without myopia.

Dry KL, Van Dorp DB, Aldred MA, Brown J, Hardwick LJ, Wright AF. Dry KL, et al. Among authors: hardwick lj. Clin Genet. 1993 May;43(5):250-4. doi: 10.1111/j.1399-0004.1993.tb03812.x. Clin Genet. 1993. PMID: 8375106

6

Analysis of three deletion breakpoints in Xp21.1 and the further localization of RP3.

Brown J, Dry KL, Edgar AJ, Pryde FE, Hardwick LJ, Aldred MA, Lester DH, Boyle S, Kaplan J, Dufier JL, Ho MF, Monaco AM, Musarella MA, Wright AF. Brown J, et al. Among authors: hardwick lj. Genomics. 1996 Oct 15;37(2):200-10. doi: 10.1006/geno.1996.0543. Genomics. 1996. PMID: 8921393

7

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: hardwick lj. Genomics. 1992 Sep;14(1):99-104. doi: 10.1016/s0888-7543(05)80289-7. Genomics. 1992. PMID: 1427834

8

A simple method for rapid isolation of microsatellites from yeast artificial chromosomes.

Brown J, Hardwick LJ, Wright AF. Brown J, et al. Among authors: hardwick lj. Mol Cell Probes. 1995 Feb;9(1):53-7. doi: 10.1016/s0890-8508(95)91022-0. Mol Cell Probes. 1995. PMID: 7760861

9

Linkage of the gene that encodes the alpha 1 chain of type V collagen (COL5A1) to type II Ehlers-Danlos syndrome (EDS II).

Loughlin J, Irven C, Hardwick LJ, Butcher S, Walsh S, Wordsworth P, Sykes B. Loughlin J, et al. Among authors: hardwick lj. Hum Mol Genet. 1995 Sep;4(9):1649-51. doi: 10.1093/hmg/4.9.1649. Hum Mol Genet. 1995. PMID: 8541855

10

Genetic mapping of susceptibility loci in the genes involved in rheumatoid arthritis.

Hardwick LJ, Walsh S, Butcher S, Nicod A, Shatford J, Bell J, Lathrop M, Wordsworth BP. Hardwick LJ, et al. J Rheumatol. 1997 Jan;24(1):197-8. J Rheumatol. 1997. PMID: 9002037

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