Clayton JF - Search Results

1

Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14.

Wright AF, Bhattacharya SS, Clayton JF, Dempster M, Tippett P, McKeown CM, Jay M, Jay B, Bird AC. Wright AF, et al. Among authors: clayton jf. Am J Hum Genet. 1987 Oct;41(4):635-44. Am J Hum Genet. 1987. PMID: 3477957 Free PMC article.

2

Studies of genetic linkage between adult polycystic kidney disease and three markers on chromosome 16.

Watson ML, Wright AF, Macnicol AM, Allan PL, Clayton JF, Dempster M, Jeremiah SJ, Corney G, Hopkinson DA. Watson ML, et al. Among authors: clayton jf. J Med Genet. 1987 Aug;24(8):457-61. doi: 10.1136/jmg.24.8.457. J Med Genet. 1987. PMID: 2821260 Free PMC article.

3

Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 (L1.28): further linkage data, heterogeneity testing, and risk estimation.

Clayton JF, Wright AF, Jay M, McKeown CM, Dempster M, Jay BS, Bird AC, Bhattacharya SS. Clayton JF, et al. Hum Genet. 1986 Oct;74(2):168-71. doi: 10.1007/BF00282083. Hum Genet. 1986. PMID: 2876947

4

A genetic linkage study of choroideremia.

Jay M, Wright AF, Clayton JF, Deans M, Dempster M, Bhattacharya SS, Jay B. Jay M, et al. Among authors: clayton jf. Ophthalmic Paediatr Genet. 1986 Dec;7(3):201-4. doi: 10.3109/13816818609004139. Ophthalmic Paediatr Genet. 1986. PMID: 2882457

5

A genetic linkage study of a kindred with X-linked retinitis pigmentosa.

Bhattacharya SS, Clayton JF, Harper PS, Hoare GW, Jay MR, Lyness AL, Wright AF. Bhattacharya SS, et al. Among authors: clayton jf. Br J Ophthalmol. 1985 May;69(5):340-7. doi: 10.1136/bjo.69.5.340. Br J Ophthalmol. 1985. PMID: 3994951 Free PMC article.

6

Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28.

Bhattacharya SS, Wright AF, Clayton JF, Price WH, Phillips CI, McKeown CM, Jay M, Bird AC, Pearson PL, Southern EM, et al. Bhattacharya SS, et al. Among authors: clayton jf. Nature. 1984 May 17-23;309(5965):253-5. doi: 10.1038/309253a0. Nature. 1984. PMID: 6325945

7

Linkage heterogeneity and fragile X.

Clayton JF, Gosden CM, Hastie ND, Evans HJ. Clayton JF, et al. Hum Genet. 1988 Apr;78(4):338-42. doi: 10.1007/BF00291731. Hum Genet. 1988. PMID: 2896154

8

Multipoint linkage analysis of steroid sulfatase (X-linked ichthyosis) and distal Xp markers.

Yates JR, Goudie DR, Gillard EF, Aitken DA, Affara NA, Clayton JF, Tippett PA, Ferguson-Smith MA. Yates JR, et al. Among authors: clayton jf. Genomics. 1987 Sep;1(1):52-9. doi: 10.1016/0888-7543(87)90104-2. Genomics. 1987. PMID: 3478297

9

Ten families with fragile X syndrome: linkage relationships with four DNA probes from distal Xq.

Buchanan JA, Buckton KE, Gosden CM, Newton MS, Clayton JF, Christie S, Hastie N. Buchanan JA, et al. Among authors: clayton jf. Hum Genet. 1987 Jun;76(2):165-72. doi: 10.1007/BF00284915. Hum Genet. 1987. PMID: 3038730

10

A multipoint linkage analysis program for X-linked disorders, with the example of Duchenne muscular dystrophy and seven DNA probes.

Clayton J. Clayton J. Hum Genet. 1986 May;73(1):68-72. doi: 10.1007/BF00292667. Hum Genet. 1986. PMID: 3458666

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