Evans DG - Search Results

1

Are there low-penetrance TP53 Alleles? evidence from childhood adrenocortical tumors.

Varley JM, McGown G, Thorncroft M, James LA, Margison GP, Forster G, Evans DG, Harris M, Kelsey AM, Birch JM. Varley JM, et al. Among authors: evans dg. Am J Hum Genet. 1999 Oct;65(4):995-1006. doi: 10.1086/302575. Am J Hum Genet. 1999. PMID: 10486318 Free PMC article.

2

A linkage study in seven breast cancer families.

Teare MD, Santibáñez-Koref MF, Wallace SA, White GR, Evans DG, Burnell LD, Harris M, Howell A, Birch JM. Teare MD, et al. Among authors: evans dg. Am J Hum Genet. 1993 Apr;52(4):786-8. Am J Hum Genet. 1993. PMID: 8460644 Free PMC article.

3

A previously undescribed mutation within the tetramerisation domain of TP53 in a family with Li-Fraumeni syndrome.

Varley JM, McGown G, Thorncroft M, Cochrane S, Morrison P, Woll P, Kelsey AM, Mitchell EL, Boyle J, Birch JM, Evans DG. Varley JM, et al. Among authors: evans dg. Oncogene. 1996 Jun 6;12(11):2437-42. Oncogene. 1996. PMID: 8649785

4

A novel deletion within exon 6 of TP53 in a family with Li-Fraumeni-like syndrome, and LOH in a benign lesion from a mutation carrier.

Varley JM, Thorncroft M, McGown G, Tricker K, Birch JM, Evans DG. Varley JM, et al. Among authors: evans dg. Cancer Genet Cytogenet. 1996 Aug;90(1):14-6. doi: 10.1016/0165-4608(96)00059-3. Cancer Genet Cytogenet. 1996. PMID: 8780740

5

An extended Li-Fraumeni kindred with gastric carcinoma and a codon 175 mutation in TP53.

Varley JM, McGown G, Thorncroft M, Tricker KJ, Teare MD, Santibanez-Koref MF, Martin J, Birch JM, Evans DG. Varley JM, et al. Among authors: evans dg. J Med Genet. 1995 Dec;32(12):942-5. doi: 10.1136/jmg.32.12.942. J Med Genet. 1995. PMID: 8825920 Free PMC article.

6

Mutation screening of MSH2 and MLH1 mRNA in hereditary non-polyposis colon cancer syndrome.

Froggatt NJ, Brassett C, Koch DJ, Evans DG, Hodgson SV, Ponder BA, Maher ER. Froggatt NJ, et al. Among authors: evans dg. J Med Genet. 1996 Sep;33(9):726-30. doi: 10.1136/jmg.33.9.726. J Med Genet. 1996. PMID: 8880570 Free PMC article.

7

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: evans dg. 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.

8

Microsatellite instability in early onset and familial colorectal cancer.

Brassett C, Joyce JA, Froggatt NJ, Williams G, Furniss D, Walsh S, Miller R, Evans DG, Maher ER. Brassett C, et al. Among authors: evans dg. J Med Genet. 1996 Dec;33(12):981-5. doi: 10.1136/jmg.33.12.981. J Med Genet. 1996. PMID: 9004127 Free PMC article.

9

A detailed study of loss of heterozygosity on chromosome 17 in tumours from Li-Fraumeni patients carrying a mutation to the TP53 gene.

Varley JM, Thorncroft M, McGown G, Appleby J, Kelsey AM, Tricker KJ, Evans DG, Birch JM. Varley JM, et al. Among authors: evans dg. Oncogene. 1997 Feb 20;14(7):865-71. doi: 10.1038/sj.onc.1201041. Oncogene. 1997. PMID: 9047394

10

Li-Fraumeni syndrome--a molecular and clinical review.

Varley JM, Evans DG, Birch JM. Varley JM, et al. Among authors: evans dg. Br J Cancer. 1997;76(1):1-14. doi: 10.1038/bjc.1997.328. Br J Cancer. 1997. PMID: 9218725 Free PMC article. Review. No abstract available.

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