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Lohman, F.
( F. Lohman)
cancer breast cancer breast variant family subject control r 117g breast cancer cases individual chek 2 brca 1 mutation susceptibility chek 2 variants kingdom i 157t sequence variant evaluation age 60 years breast cancer susceptibility control subjects breast cancer risk netherland genetic fha domain frequency study breast cancer incidence genet research variant ascertainment analysis li-fraumeni syndrome germline consortium 1100 delc syndrome binding family history america netherlands domain kinase america table evaluation pedigree phosphorylation case subjects control individuals dna damage response r 117a cancer research u.k r 145w population 1/723 control subjects checkpoint r 117g variant 723 control subjects contribution ascertainment chk 2 gene damage 2/737 brca 1/2-negative chk 2 brca 2 mutations allele 1/2-negative brca 1/brca 2-breast vahteristo protein genomic project wild-type institute linkage analyses dutch li-fraumeni
1 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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