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

Paula S. Felicio, Rebeca S. Grasel, Natalia Campacci, Andre E. de Paula, Henrique C.R. Galvão, Giovana T. Torrezan, Cristina S. Sabato, Gabriela C. Fernandes, Cristiano P. Souza, Rodrigo D. Michelli, Carlos E. Andrade, Bruna Durães De Figueiredo Barros, Marcus M. Matsushita, Timothée Revil, Jiannis Ragoussis, Fergus J. Couch, Steven N. Hart, Rui M. Reis, Matias E. Melendez, Patricia N. ToninDirce M. Carraro, Edenir I. Palmero

Research output: Contribution to journal › Article › peer-review

2 Scopus citations

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Medicine & Life Sciences