The CHEK2 1100delC Mutation Identifies Families with a Hereditary Breast and Colorectal Cancer Phenotype-Reference-Cited by-同舟云学术

The CHEK2 1100delC Mutation Identifies Families with a Hereditary Breast and Colorectal Cancer Phenotype

Published:2003-05 Issue:5 Volume:72 Page:1308-1314
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Meijers-Heijboer Hanne,Wasielewski Marijke,Wagner Anja,Hollestelle Antoinette,Elstrodt Fons,van den Bos Renate,de Snoo Anja,Tjon A Fat Grace,Brekelmans Cecile,Jagmohan Shantie,Franken Patrick,Verkuijlen Paul,van den Ouweland Ans,Chapman Pamela,Tops Carli,Möslein Gabriela,Burn John,Lynch Henry,Klijn Jan,Fodde Riccardo,Wijnen Juul,Vasen Hans,Schutte Mieke

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference17 articles.

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4. Tumor variation in families with breast cancer;Lynch;JAMA,1972

5. Meijers-Heijboer H, Brekelmans CTM, Menke-Pluymers M, Seynaeve C, Baalbergen A, Burger C, Crepin E, van den Ouweland AWM, van Geel B, Klijn JGM. Use of genetic testing and prophylactic mastectomy and oophorectomy in women with breast cancer and/or ovarian cancer from families with a BRCA1 or BRCA2 mutation. J Clin Oncol (in press).

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