Works matching AU Galvão, Henrique C. R.

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