Payne SJ - Search Results

1

Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations.

Maher ER, Webster AR, Richards FM, Green JS, Crossey PA, Payne SJ, Moore AT. Maher ER, et al. Among authors: payne sj. J Med Genet. 1996 Apr;33(4):328-32. doi: 10.1136/jmg.33.4.328. J Med Genet. 1996. PMID: 8730290 Free PMC article.

2

Presymptomatic diagnosis of von Hippel-Lindau disease with flanking DNA markers.

Maher ER, Bentley E, Payne SJ, Latif F, Richards FM, Chiano M, Hosoe S, Yates JR, Linehan M, Barton DE, et al. Maher ER, et al. Among authors: payne sj. J Med Genet. 1992 Dec;29(12):902-5. doi: 10.1136/jmg.29.12.902. J Med Genet. 1992. PMID: 1362224 Free PMC article.

3

A PCR generated AccI RFLP in the 3' untranslated region of the von Hippel-Lindau disease (VHL) tumour suppressor gene.

Payne SJ, Richards FM, Maher ER. Payne SJ, et al. Hum Mol Genet. 1994 Feb;3(2):390. doi: 10.1093/hmg/3.2.390. Hum Mol Genet. 1994. PMID: 7911705 No abstract available.

4

Evaluation of molecular genetic diagnosis in the management of familial adenomatous polyposis coli: a population based study.

Maher ER, Barton DE, Slatter R, Koch DJ, Jones MH, Nagase H, Payne SJ, Charles SJ, Moore AT, Nakamura Y, et al. Maher ER, et al. Among authors: payne sj. J Med Genet. 1993 Aug;30(8):675-8. doi: 10.1136/jmg.30.8.675. J Med Genet. 1993. PMID: 8105087 Free PMC article.

5

Molecular analysis of de novo germline mutations in the von Hippel-Lindau disease gene.

Richards FM, Payne SJ, Zbar B, Affara NA, Ferguson-Smith MA, Maher ER. Richards FM, et al. Among authors: payne sj. Hum Mol Genet. 1995 Nov;4(11):2139-43. doi: 10.1093/hmg/4.11.2139. Hum Mol Genet. 1995. PMID: 8589692

6

A genetic register for von Hippel-Lindau disease.

Maddock IR, Moran A, Maher ER, Teare MD, Norman A, Payne SJ, Whitehouse R, Dodd C, Lavin M, Hartley N, Super M, Evans DG. Maddock IR, et al. Among authors: payne sj. J Med Genet. 1996 Feb;33(2):120-7. doi: 10.1136/jmg.33.2.120. J Med Genet. 1996. PMID: 8929948 Free PMC article.

7

Molecular genetic analysis of the 3p- syndrome.

Phipps ME, Latif F, Prowse A, Payne SJ, Dietz-Band J, Leversha M, Affara NA, Moore AT, Tolmie J, Schinzel A, et al. Phipps ME, et al. Among authors: payne sj. Hum Mol Genet. 1994 Jun;3(6):903-8. doi: 10.1093/hmg/3.6.903. Hum Mol Genet. 1994. PMID: 7951234 Free article. Clinical Trial.

8

Improved genetic mapping of X linked retinoschisis.

George ND, Payne SJ, Bill RM, Barton DE, Moore AT, Yates JR. George ND, et al. Among authors: payne sj. J Med Genet. 1996 Nov;33(11):919-22. doi: 10.1136/jmg.33.11.919. J Med Genet. 1996. PMID: 8950671 Free PMC article.

9

Contribution of cyclin d1 (CCND1) and E-cadherin (CDH1) polymorphisms to familial and sporadic colorectal cancer.

Porter TR, Richards FM, Houlston RS, Evans DG, Jankowski JA, Macdonald F, Norbury G, Payne SJ, Fisher SA, Tomlinson I, Maher ER. Porter TR, et al. Among authors: payne sj. Oncogene. 2002 Mar 14;21(12):1928-33. doi: 10.1038/sj.onc.1205245. Oncogene. 2002. PMID: 11896626 Clinical Trial.

10

von Hippel-Lindau disease and familial polyposis coli in the same family.

Kilmartin DJ, Mooney DJ, Acheson RW, Payne SJ, Maher ER, Eustace P. Kilmartin DJ, et al. Among authors: payne sj. Arch Ophthalmol. 1996 Oct;114(10):1294. doi: 10.1001/archopht.1996.01100140494034. Arch Ophthalmol. 1996. PMID: 8859104 No abstract available.

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