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

✍ Scribed by Ruijs, Marielle W.G. (author);Verhoef, Senno (author);Rookus, Matti A. (author);Pruntel, Roelof (author);Van Der Hout, Annemarie H. (author);Hogervorst, Frans B.L. (author);Kluijt, I. (author);Sijmons, Rolf H. (author);Aalfs, Cora M. (author);Wagner, Anja (author);Ausems, Margreet G.E.M. (author);Hoogerbrugge, Nicoline (author);Van Asperen, Christi J. (author);Gomez Garcia, Encarna B. (author);Meijers-Heijboer, Hanne (author);Ten Kate, Leo P. (author);Menko, Fred H. (author);Van 'T Veer, Laura J. (author)

Book ID: 115510326
Publisher: BMJ Publishing Group
Year: 2010
Tongue: English
Weight: 125 KB
Volume: 47
Category: Article
ISSN: 0022-2593
DOI: 10.1136/jmg.2009.073429

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