TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes

M.W.G. Ruijs, S Verhoef, M.A. Rookus, R Pruntel, A.H. van der Hout, F.B.L. Hogervorst, I Kluijt, RH Sijmons, C.M. Aalfs, A. Wagner, M.G.E.M. Ausems, N. Hoogerbrugge, C.J. van Asperen, E.B.G. Garcia, E.J. Meijers-Heijboer, L.P. ten Kate, F.H. Menko, L.J. van 't Veer

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)421-428
JournalJournal of Medical Genetics
Issue number6
Publication statusPublished - 2010

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