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Journal of Medical Genetics|March 30, 2021
Testicular Sertoli cell tumour and potentially testicular Leydig cell tumour are features of DICER1 syndromeLisa Golmard, Lauren M Vasta, Valérie Duflos, 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.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 1, 2017
Location of Mutation in BRCA2 Gene and Survival in Patients with Ovarian CancerS Intidhar Labidi-Galy, Timothée Olivier, Manuel Rodrigues, et al.
Gynecologic Oncology|October 13, 2019
Clinical factors associated with prolonged response and survival under olaparib as maintenance therapy in BRCA mutated ovarian cancersS Intidhar Labidi-Galy, Thibault de La Motte Rouge, Olfa Derbel, 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.
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.
Clinical Genetics|January 17, 2021
Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic ConsortiumFlavie Boulouard, Edwige Kasper, Marie-Pierre Buisine, 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.
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.
JAMA Ophthalmology|June 18, 2025
Uveal Melanoma and the Lynch Syndrome Tumor SpectrumAnaïs Le Ven, Marie-Charlotte Villy, André Bortolini Silveira, et al.
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