Wright AF - Search Results

1

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: wright af. 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.

2

Effects of angiotensin converting enzyme inhibition in adult polycystic kidney disease.

Watson ML, Macnicol AM, Allan PL, Wright AF. Watson ML, et al. Among authors: wright af. Kidney Int. 1992 Jan;41(1):206-10. doi: 10.1038/ki.1992.28. Kidney Int. 1992. PMID: 1317477 Free article.

3

Multipoint mapping of adult onset polycystic kidney disease (PKD1) on chromosome 16.

Pignatelli PM, Pound SE, Carothers AD, Macnicol AM, Allan PL, Watson ML, Wright AF. Pignatelli PM, et al. Among authors: wright af. J Med Genet. 1992 Sep;29(9):638-41. doi: 10.1136/jmg.29.9.638. J Med Genet. 1992. PMID: 1404294 Free PMC article.

4

Evidence for linkage disequilibrium between D16S94 and the adult onset polycystic kidney disease (PKD1) gene.

Pound SE, Carothers AD, Pignatelli PM, Macnicol AM, Watson ML, Wright AF. Pound SE, et al. Among authors: wright af. J Med Genet. 1992 Apr;29(4):247-8. doi: 10.1136/jmg.29.4.247. J Med Genet. 1992. PMID: 1583644 Free PMC article. No abstract available.

5

Education and attitudes in families with adult polycystic kidney disease.

Macnicol AM, Wright AF, Watson ML. Macnicol AM, et al. Among authors: wright af. Nephrol Dial Transplant. 1991;6(1):27-30. doi: 10.1093/ndt/6.1.27. Nephrol Dial Transplant. 1991. PMID: 2057113

6

Adult polycystic kidney disease.

Watson ML, Macnicol AM, Wright AF. Watson ML, et al. Among authors: wright af. BMJ. 1990 Jan 13;300(6717):62-3. doi: 10.1136/bmj.300.6717.62. BMJ. 1990. PMID: 2105771 Free PMC article. Review. No abstract available.

7

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. Am J Hum Genet. 1987 Oct;41(4):635-44. Am J Hum Genet. 1987. PMID: 3477957 Free PMC article.

8

Haplotype analysis in autosomal dominant polycystic kidney disease.

Pound SE, Thomas S, Snarey A, Macnicol AM, Watson ML, Pignatelli PM, Frischauf AM, Harris PC, Wright AF. Pound SE, et al. Among authors: wright af. J Med Genet. 1995 Mar;32(3):208-12. doi: 10.1136/jmg.32.3.208. J Med Genet. 1995. PMID: 7783171 Free PMC article.

9

A study of genetic linkage heterogeneity in 35 adult-onset polycystic kidney disease families.

Wright AF, Teague PW, Pound SE, Pignatelli PM, Macnicol AM, Carothers AD, De Mey RJ, Allan PL, Watson ML. Wright AF, et al. Hum Genet. 1993 Jan;90(5):569-71. doi: 10.1007/BF00217461. Hum Genet. 1993. PMID: 8428756

10

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. Among authors: wright af. Hum Genet. 1986 Oct;74(2):168-71. doi: 10.1007/BF00282083. Hum Genet. 1986. PMID: 2876947

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