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Breast (Edinburgh, Scotland)|March 2, 2019
"Decoding hereditary breast cancer" benefits and questions from multigene panel testingChrystelle Colas, Lisa Golmard, Antoine de Pauw, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 14, 2012
BRCA1/2 carriers: their childbearing plans and theoretical intentions about having preimplantation genetic diagnosis and prenatal diagnosisClaire Julian-Reynier, Roxane Fabre, Isabelle Coupier, et al.American Journal of Clinical Oncology|March 25, 2009
Familial breast cancer: clinical response to induction chemotherapy or radiotherapy related to BRCA1/2 mutations statusAlain Fourquet, Dominique Stoppa-Lyonnet, Youlia M Kirova, et al.Familial Cancer|May 8, 2004
BRCA1 testing in breast and/or ovarian cancer families from northeastern France identifies two common mutations with a founder effectDanièle Muller, Catherine Bonaiti-Pellié, Joseph Abecassis, et al.Breast Cancer Research and Treatment|July 16, 2011
Variation in breast cancer risk with mutation position, smoking, alcohol, and chest X-ray history, in the French National BRCA1/2 carrier cohort (GENEPSO)Julie Lecarpentier, Catherine Noguès, Emmanuelle Mouret-Fourme, et al.Human Molecular Genetics|October 24, 2002
The nonsense-mediated mRNA decay pathway triggers degradation of most BRCA1 mRNAs bearing premature termination codonsLaure Perrin-Vidoz, Olga M Sinilnikova, Dominique Stoppa-Lyonnet, et al.Bulletin Du Cancer|May 30, 2012
[Perception accuracy of BRCA1/2 mutation predisposition in breast cancer women and associated factors]Débora Leblond, Anne Brédart, Sylvie Dolbeault, et al.Bulletin Du Cancer|February 25, 2012
[Hereditary forms of ovarian cancer]Antoine de Pauw, Laurianne Jolissaint, Paul Fréneaux, et al.International Journal of Cancer|May 7, 2002
Variation in breast cancer risk of heterozygotes for ataxia-telangiectasia according to environmental factorsBéatrice Geoffroy-Perez, Nicolas Janin, Katia Ossian, et al.Pageof 36