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cancer breast cancer breast family brca 1 brca 2 mutations mutation chek 2*1100delc variant individual 2*1100delc control chek 2 frequency susceptibility subject breast cancer risk netherland genetic r 117g breast cancer susceptibility research analysis sequence breast cancer cases study allele nature population linkage breast cancer incidence chek 2 variants kingdom control individuals li-fraumeni syndrome family history carrier brca 2 i 157t kinase america syndrome table variant evaluation age 60 years breast cancer unselected control subjects analyses series chk 2 genomic checkpoint institute pedigree damage group chromosome protein fha domain dutch marker genome 1100 delc mutation genet chek 2*1100delc variant variant ascertainment germline consortium 1100 delc binding fi rst america netherlands domain heteroduplex analysis estimate segregation evaluation phosphorylation model case subjects
2 Most Recent Publications
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Variants in CHEK2 other than 1100delC do not make a major contribution to breast cancer susceptibility
(Article)
Schutte, A.E.M. Meijers-Heijboer, E.J. Nathanson, K.L. Futreal, P.A. Stratton, M.R. Seal, S. Barfoot, R. Ouweland, A.M.W. van den Klijn, J.G.M. Easton, D.F. Wasielewski, M. Evans, D.G. Eccles, D. Weber, B.L. Rahman, N. Meijers, C. Lohman, F. |
2003-01-01
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Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations
(Article)
Meijers-Heijboer, E.J. Snoo, A. de Schutte, M. McGuffog, L. Thompson, D. Easton, D.F. Sodha, N. Seal, S. Barfoot, R. Mangion, J. Chang-Claude, J. Eccles, D. Oldenburg, R. Eeles, R. Evans, D.G. Houlston, R. Murday, V. Narod, S. Peretz, T. Peto, J. Phelan, C. Zhang, H.X. Szabo, C. Hollestelle, A. Devilee, P. Goldgar, D. Futreal, P.A. Nathanson, K.L. Weber, B.L. Rahman, N. Stratton, M.R. Ouweland, A.M.W. van den Klijn, J.G.M. Wasielewski, M. Houben, M. Elstrodt, F. Crepin, E. Veghel-Plandsoen, M. van Duijn, C.M. van Bartels, C.C.M. Meijers, C. |
2002-05-01
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