Ponder BA - Search Results

1

Cowden syndrome and Lhermitte-Duclos disease in a family: a single genetic syndrome with pleiotropy?

Eng C, Murday V, Seal S, Mohammed S, Hodgson SV, Chaudary MA, Fentiman IS, Ponder BA, Eeles RA. Eng C, et al. Among authors: ponder ba. J Med Genet. 1994 Jun;31(6):458-61. doi: 10.1136/jmg.31.6.458. J Med Genet. 1994. PMID: 8071972 Free PMC article.

2

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: ponder ba. 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.

3

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: ponder ba. 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.

4

Haplotype analysis of MEN 2 mutations.

Gardner E, Mulligan LM, Eng C, Healey CS, Kwok JB, Ponder MA, Ponder BA. Gardner E, et al. Among authors: ponder ba, ponder ma. Hum Mol Genet. 1994 Oct;3(10):1771-4. doi: 10.1093/hmg/3.10.1771. Hum Mol Genet. 1994. PMID: 7849700

5

The role of gene mutations in the genesis of familial cancers.

Eng C, Ponder BA. Eng C, et al. Among authors: ponder ba. FASEB J. 1993 Jul;7(10):910-9. doi: 10.1096/fasebj.7.10.8102106. FASEB J. 1993. PMID: 8102106 Review.

6

Molecular genetic diagnosis of von Hippel-Lindau disease in familial phaeochromocytoma.

Crossey PA, Eng C, Ginalska-Malinowska M, Lennard TW, Wheeler DC, Ponder BA, Maher ER. Crossey PA, et al. Among authors: ponder ba. J Med Genet. 1995 Nov;32(11):885-6. doi: 10.1136/jmg.32.11.885. J Med Genet. 1995. PMID: 8592333 Free PMC article.

7

Localization of the gene for Cowden disease to chromosome 10q22-23.

Nelen MR, Padberg GW, Peeters EA, Lin AY, van den Helm B, Frants RR, Coulon V, Goldstein AM, van Reen MM, Easton DF, Eeles RA, Hodgsen S, Mulvihill JJ, Murday VA, Tucker MA, Mariman EC, Starink TM, Ponder BA, Ropers HH, Kremer H, Longy M, Eng C. Nelen MR, et al. Among authors: ponder ba. Nat Genet. 1996 May;13(1):114-6. doi: 10.1038/ng0596-114. Nat Genet. 1996. PMID: 8673088 Free article.

8

Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene.

Gayther SA, Mangion J, Russell P, Seal S, Barfoot R, Ponder BA, Stratton MR, Easton D. Gayther SA, et al. Among authors: ponder ba. Nat Genet. 1997 Jan;15(1):103-5. doi: 10.1038/ng0197-103. Nat Genet. 1997. PMID: 8988179

9

Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL.

Woodward ER, Eng C, McMahon R, Voutilainen R, Affara NA, Ponder BA, Maher ER. Woodward ER, et al. Among authors: ponder ba. Hum Mol Genet. 1997 Jul;6(7):1051-6. doi: 10.1093/hmg/6.7.1051. Hum Mol Genet. 1997. PMID: 9215674

10

Familial cancer syndromes.

Eng C, Stratton M, Ponder B, Murday V, Easton D, Sacks N, Watson M, Eeles R. Eng C, et al. Lancet. 1994 Mar 19;343(8899):709-13. doi: 10.1016/s0140-6736(94)91585-7. Lancet. 1994. PMID: 7907684 No abstract available.

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