1. Whole‐exome sequencing of non‐BRCA1/BRCA2 mutation carrier cases at high‐risk for hereditary breast/ovarian cancer. Issue 3 (28th December 2020) Authors: Felicio, Paula S.; Grasel, Rebeca S.; Campacci, Natalia; de 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, ... Journal: Human mutation Issue: Volume 42:Issue 3(2021) Page Start: 290 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗