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JMIR Research Protocols|September 22, 2017
Cancer Predisposition Cascade Screening for Hereditary Breast/Ovarian Cancer and Lynch Syndromes in Switzerland: Study ProtocolMaria C Katapodi, Valeria Viassolo, Maria Caiata-Zufferey, 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.Public Health Genomics|January 30, 2019
Challenges and Opportunities for Cancer Predisposition Cascade Screening for Hereditary Breast and Ovarian Cancer and Lynch Syndrome in Switzerland: Findings from an International WorkshopChristos Nikolaidis, Chang Ming, Carla Pedrazzani, et al.Journal of Medical Genetics|May 12, 2017
The BRCA1 c. 5096G>A p.Arg1699Gln (R1699Q) intermediate risk variant: breast and ovarian cancer risk estimation and recommendations for clinical management from the ENIGMA consortiumSetareh Moghadasi, Huong D Meeks, Maaike Pg Vreeswijk, et al.Human Molecular Genetics|July 2, 2015
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factorPaolo Peterlongo, Irene Catucci, Mara Colombo, et al.Pageof 3