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Genes, Chromosomes & Cancer|December 11, 2022
AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancerJulie Leclerc, Marie Beaumont, Roseline Vibert, et al.Neuro-Oncology|September 11, 2019
Medulloblastomas associated with an APC germline pathogenic variant share the good prognosis of CTNNB1-mutated medulloblastomasAurore Surun, Pascale Varlet, Laurence Brugières, et al.European Journal of Human Genetics : EJHG|October 3, 2025
Myeloid neoplasms risks for germline DDX41 pathogenic variants carriersMarie-Charlotte Villy, Youenn Drouet, Lise Larcher, et al.Breast (Edinburgh, Scotland)|December 7, 2023
Clinical implications of incorporating genetic and non-genetic risk factors in CanRisk-based breast cancer risk predictionAnja Tüchler, Antoine De Pauw, Corinna Ernst, et al.JCO Precision Oncology|June 1, 2023
Mismatch Repair Deficiency and Lynch Syndrome Among Adult Patients With GliomaPatrick R Benusiglio, Fikret Elder, Mehdi Touat, et al.Frontiers in Immunology|July 18, 2018
No Overt Clinical Immunodeficiency Despite Immune Biological Abnormalities in Patients With Constitutional Mismatch Repair DeficiencyVictoria K Tesch, Hanna IJspeert, Andrea Raicht, et al.JAMA Ophthalmology|June 18, 2025
Uveal Melanoma and the Lynch Syndrome Tumor SpectrumAnaïs Le Ven, Marie-Charlotte Villy, André Bortolini Silveira, et al.Journal of Medical Genetics|August 29, 2022
First estimates of diffuse gastric cancer risks for carriers of CTNNA1 germline pathogenic variantsMarie Coudert, Youenn Drouet, Hélène Delhomelle, et al.Pediatric Blood & Cancer|September 20, 2024
Comprehensive analysis of constitutional mismatch repair deficiency-associated non-Hodgkin lymphomas in a global cohortCharlotte Rigaud, Victoria J Forster, Hiba Al-Tarrah, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 29, 2026
Cancer risks for ATM variant heterozygotesYue Jiao, David E Goldgar, Dorothée Le Gal, et al.Pageof 12