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Familial Cancer|August 13, 2013
Cancer risk and genotype-phenotype correlations in PTEN hamartoma tumor syndromeMarry H Nieuwenhuis, C Marleen Kets, Maureen Murphy-Ryan, et al.Human Mutation|May 18, 2026
MLH1 Constitutional Epimutation Screening Requires Highly Sensitive Assays to Identify Lynch Syndrome Patients With Very Low Mosaic Methylation LevelCédric Facon, Catherine Vermaut, Lucie Delattre, et al.European Journal of Human Genetics : EJHG|April 23, 2023
Lynch syndrome: influence of additional susceptibility variants on cancer riskRoseline Vibert, Jasmine Hasnaoui, Alexandre Perrier, et al.Breast (Edinburgh, Scotland)|December 14, 2023
Male breast cancer: No evidence for mosaic BRCA1 promoter methylation involvementMathias Schwartz, Sabrina Ibadioune, Sophie Vacher, et al.Journal of Medical Genetics|July 4, 2023
MSH3: a confirmed predisposing gene for adenomatous polyposisMarie-Charlotte Villy, Julien Masliah-Planchon, Anne Schnitzler, et al.JAMA|June 7, 2011
Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndromeValérie Bonadona, Bernard Bonaïti, Sylviane Olschwang, et al.Breast Cancer Research : BCR|July 6, 2012
Variation in breast cancer risk associated with factors related to pregnancies according to truncating mutation location, in the French National BRCA1 and BRCA2 mutations carrier cohort (GENEPSO)Julie Lecarpentier, Catherine Noguès, Emmanuelle Mouret-Fourme, et al.Journal of the National Cancer Institute|September 20, 2017
The Balance Between Cytotoxic T-cell Lymphocytes and Immune Checkpoint Expression in the Prognosis of Colon TumorsLaetitia Marisa, Magali Svrcek, Ada Collura, et al.Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|January 24, 2015
Breast Cancer Risk Associated with Estrogen Exposure and Truncating Mutation Location in BRCA1/2 CarriersJulie Lecarpentier, Catherine Noguès, Emmanuelle Mouret-Fourme, et al.Journal of the National Cancer Institute|December 7, 2023
Familial uveal melanoma and other tumors in 25 families with monoallelic germline MBD4 variantsMarie-Charlotte Villy, Anaïs Le Ven, Marine Le Mentec, et al.Pageof 12