Evans DG - Search Results

1

Familial infiltrative fibromatosis (desmoid tumours) (MIM135290) caused by a recurrent 3' APC gene mutation.

Scott RJ, Froggatt NJ, Trembath RC, Evans DG, Hodgson SV, Maher ER. Scott RJ, et al. Among authors: evans dg. Hum Mol Genet. 1996 Dec;5(12):1921-4. doi: 10.1093/hmg/5.12.1921. Hum Mol Genet. 1996. PMID: 8968744

2

Molecular genetic analysis of exons 1 to 6 of the APC gene in non-polyposis familial colorectal cancer.

Joyce JA, Froggatt NJ, Davies R, Evans DG, Trembath R, Barton DE, Maher ER. Joyce JA, et al. Among authors: evans dg. Clin Genet. 1995 Dec;48(6):299-303. doi: 10.1111/j.1399-0004.1995.tb04113.x. Clin Genet. 1995. PMID: 8835324

3

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.

4

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.

5

Germline E-cadherin gene (CDH1) mutations predispose to familial gastric cancer and colorectal cancer.

Richards FM, McKee SA, Rajpar MH, Cole TR, Evans DG, Jankowski JA, McKeown C, Sanders DS, Maher ER. Richards FM, et al. Among authors: evans dg. Hum Mol Genet. 1999 Apr;8(4):607-10. doi: 10.1093/hmg/8.4.607. Hum Mol Genet. 1999. PMID: 10072428

6

Genetic linkage analysis in hereditary non-polyposis colon cancer syndrome.

Froggatt NJ, Koch J, Davies R, Evans DG, Clamp A, Quarrell OW, Weissenbach J, Hodgson SV, Ponder BA, Barton DE, et al. Froggatt NJ, et al. Among authors: evans dg. J Med Genet. 1995 May;32(5):352-7. doi: 10.1136/jmg.32.5.352. J Med Genet. 1995. PMID: 7616541 Free PMC article.

7

Uptake of genetic testing for cancer predisposition.

Evans DG, Maher ER, Macleod R, Davies DR, Craufurd D. Evans DG, et al. J Med Genet. 1997 Sep;34(9):746-8. doi: 10.1136/jmg.34.9.746. J Med Genet. 1997. PMID: 9321761 Free PMC article.

8

A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, and sex specific differences in colorectal cancer.

Froggatt NJ, Green J, Brassett C, Evans DG, Bishop DT, Kolodner R, Maher ER. Froggatt NJ, et al. Among authors: evans dg. J Med Genet. 1999 Feb;36(2):97-102. J Med Genet. 1999. PMID: 10051005 Free PMC article.

9

Mononucleotide microsatellite instability and germline MSH6 mutation analysis in early onset colorectal cancer.

Verma L, Kane MF, Brassett C, Schmeits J, Evans DG, Kolodner RD, Maher ER. Verma L, et al. Among authors: evans dg. J Med Genet. 1999 Sep;36(9):678-82. J Med Genet. 1999. PMID: 10507723 Free PMC article.

10

Recurrent germline mutation in MSH2 arises frequently de novo.

Desai DC, Lockman JC, Chadwick RB, Gao X, Percesepe A, Evans DG, Miyaki M, Yuen ST, Radice P, Maher ER, Wright FA, de La Chapelle A. Desai DC, et al. Among authors: evans dg. J Med Genet. 2000 Sep;37(9):646-52. doi: 10.1136/jmg.37.9.646. J Med Genet. 2000. PMID: 10978353 Free PMC article.

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