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European Journal of Medical Genetics|October 15, 2020
MUTYH-associated polyposis: Review and update of the French recommendations established in 2012 under the auspices of the National Cancer institute (INCa)Chrystelle Colas, Valérie Bonadona, Stéphanie Baert-Desurmont, et al.
European Journal of Cancer (Oxford, England : 1990)|August 29, 2017
Hypermutated tumours in the era of immunotherapy: The paradigm of personalised medicineLaetitia Nebot-Bral, David Brandao, Loic Verlingue, et al.
European Journal of Medical Genetics|August 12, 2008
Proximal 15q familial euchromatic variant and PWS/AS critical region duplication in the same patient: a cytogenetic pitfallNadège Carelle-Calmels, Françoise Girard-Lemaire, Eric Guérin, et al.
The Breast Journal|September 21, 2017
Efficacy of anthracycline/taxane-based neo-adjuvant chemotherapy on triple-negative breast cancer in BRCA1/BRCA2 mutation carriersLucie Bignon, Jean-Pierre Fricker, Catherine Nogues, 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.
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.
European Journal of Human Genetics : EJHG|April 25, 2013
Germline copy number variation of genes involved in chromatin remodelling in families suggestive of Li-Fraumeni syndrome with brain tumoursJuliette Aury-Landas, Gaëlle Bougeard, Hélène Castel, et al.
Gynecologic Oncology|October 16, 2020
Impact of young age on platinum response in women with epithelial ovarian cancer: Results of a large single-institution registryJudith Michels, Catherine Genestie, Ariane Dunant, et al.
Journal of Medical Genetics|April 17, 2014
Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium 'care for CMMRD' (C4CMMRD)Katharina Wimmer, Christian P Kratz, Hans F A Vasen, et al.
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