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Clinical Genetics|March 30, 2011
Frequent mutation in North African patients with MUTYH-associated polyposisJ H Lefevre, C Colas, F Coulet, et al.
American Journal of Human Genetics|February 1, 1996
Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international studyS L Neuhausen, S Mazoyer, L Friedman, et al.
Oncogene|June 2, 2015
Breast and ovarian cancer predisposition due to de novo BRCA1 and BRCA2 mutationsL Golmard, C Delnatte, A Laugé, et al.
Clinical Genetics|April 12, 2011
Unexplained polyposis: a challenge for geneticists, pathologists and gastroenterologistsC Mongin, F Coulet, J H Lefevre, et al.
Bulletin Du Cancer|July 19, 2001
[Li-Fraumeni syndrome: update, new data and guidelines for clinical management]T Frebourg, A Abel, C Bonaiti-Pellie, et al.
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