Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleWhole‐exome sequencing of non‐BRCA1/BRCA2 mutation carrier cases at high‐risk for hereditary breast/ovarian cancer.AuthorsFelicio, Paula S.; Grasel, Rebeca S.; Campacci, Natalia; Paula, Andre E.; Galvão, Henrique C. R.; Torrezan, Giovana T.; Sabato, Cristina S.; Fernandes, Gabriela C.; Souza, Cristiano P.; Michelli, Rodrigo D.; Andrade, Carlos E.; Barros, Bruna Durães De Figueiredo; Matsushita, Marcus M.; Revil, Timothée; Ragoussis, Jiannis; Couch, Fergus J.; Hart, Steven N.; Reis, Rui M.; Melendez, Matias E.; Tonin, Patricia N.PublicationHuman Mutation, 2021, Vol 42, Issue 3, p290ISSN1059-7794Publication typeArticleDOI10.1002/humu.24158