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Familial Cancer|January 4, 2022
BRCA1 Norway: comparison of classification for BRCA1 germline variants detected in families with suspected hereditary breast and ovarian cancer between different laboratoriesHenrikke N Hovland, Rafal Al-Adhami, Sarah Louise Ariansen, et al.Familial Cancer|October 19, 2022
Next-generation universal hereditary cancer screening: implementation of an automated hereditary cancer screening program for patients with advanced cancer undergoing tumor sequencing in a large HMOTrevor L Hoffman, Hilary Kershberg, John Goff, et al.Familial Cancer|April 17, 2019
Implication of DNA repair genes in Lynch-like syndromeRosa M Xicola, Julia R Clark, Timothy Carroll, et al.Familial Cancer|April 17, 2019
Hereditary gastric cancer: what's new? Update 2013-2018Rachel S van der Post, Carla Oliveira, Parry Guilford, et al.Familial Cancer|September 26, 2018
Electronically ascertained extended pedigrees in breast cancer genetic counselingV Stefansdottir, H Skirton, O Th Johannsson, et al.Familial Cancer|June 17, 2019
Assessing a single SNP located at TERT/CLPTM1L multi-cancer risk region as a genetic modifier for risk of pancreatic cancer and melanoma in Dutch CDKN2A mutation carriersE Christodoulou, M Visser, T P Potjer, et al.Familial Cancer|June 24, 2017
Screening for Lynch syndrome in young Saudi colorectal cancer patients using microsatellite instability testing and next generation sequencingMasood Alqahtani, Caitlin Edwards, Natasha Buzzacott, et al.Familial Cancer|March 3, 2010
Prevalence of BRCA2 and CDKN2a mutations in German familial pancreatic cancer familiesEmily P Slater, Peter Langer, Volker Fendrich, et al.Familial Cancer|March 17, 2015
Pitfalls in the diagnosis of biallelic PMS2 mutationsMarina Antelo, Daniela Milito, Jennifer Rhees, et al.Familial Cancer|March 19, 2015
Clinical characterization and mutation spectrum in Caribbean Hispanic families with Lynch syndromeMarcia Cruz-Correa, Yaritza Diaz-Algorri, Julyann Pérez-Mayoral, et al.Pageof 151