Founder BRCA1 and BRCA2 Mutations in French Canadian Breast and Ovarian Cancer Families

Author:

Tonin Patricia N.,Mes-Masson Anne-Marie,Futreal P. Andrew,Morgan Kenneth,Mahon Michelle,Foulkes William D.,Cole David E.C.,Provencher Diane,Ghadirian Parviz,Narod Steven A.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference56 articles.

1. A common mutation in BRCA2 that predisposes to a variety of cancers is found in both Jewish Ashkenazi and non-Jewish individuals;Berman;Cancer Res,1996

2. Two distinct origins of a common BRCA1 mutation in breast-ovarian cancer families: a genetic study of 15 185delAG mutation kindreds;Berman;Am J Hum Genet,1996

3. Reproduction démographique et transmission génétique dans le nord-est de la province de Québec (18e-20e siècles);Bouchard;Eur J Popul,1988

4. The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac α and β myosin heavy chain genes on chromosome 14q11.2-q13;Brais;Hum Mol Genet,1995

5. The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q;Casaubon;Am J Hum Genet,1996

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