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

    Published in:
    Human Mutation, 2021, v. 42, n. 3, p. 290, doi. 10.1002/humu.24158
    By:
    • 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.
    Publication type:
    Article