Citations 1
Whole‐exome sequencing of non‐ BRCA1/BRCA2 mutation carrier cases at high‐risk for hereditary breast/ovarian cancer
Felicio, Paula Silva , Grasel, Rebeca Silveira, Campacci, Natália , Paula, Andre Escremin de, Galvão, Henrique C.R. , Torrezan, Giovana Tardin , Sabato, Cristina S., Fernandes, Gabriela Carvalho, Souza, Cristiano de Pádua , Michelli, Rodrigo D., Andrade, Carlos Eduardo Mattos Cunha , Barros, Bruna Durães de Figueiredo , Matsushita, Marcus, Revil, Timothée , Ragoussis, Jiannis , Reis, Rui Manuel , Tonin, Patricia N. , Carraro, Dirce Maria , Palmero, Edenir Inêz , Hart, Steven N , Palmero, Edenir I , Reis, Rui Manuel , Matsushita, Marcus, Couch, Fergus J. , Hart, Steven N. , Melendez, Matias Eliseo
Human Mutation | December 18, 2020 | Volume: 42 | Issue: 3 | Pages: 290-299
