Whole‐exome sequencing of non‐BRCA1/BRCA2 mutation carrier cases at high‐risk for hereditary breast/ovarian cancer

Felicio, 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. ; Carraro, Dirce M. ; Palmero, Edenir I.

Human mutation, 2021-03, Vol.42 (3), p.290-299 [Periódico revisado por pares]

United States: Hindawi Limited

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