Whole-exome sequencing of non-BRCA1/BRCA2 mutation carrier cases at high-risk for hereditary breast/ovarian cancer
对非BRCA1/BRCA2突变携带者进行全外显子组测序,这些患者罹患遗传性乳腺癌/卵巢癌的风险较高
期刊:Human Mutation
影响因子:3.7
doi:10.1002/humu.24158
Felicio, Paula S; Grasel, Rebeca S; Campacci, Natalia; de 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