학술논문
Whole-exome sequencing of non-BRCA1/BRCA2 mutation carrier cases at high-risk for hereditary breast/ovarian cancer
Document Type
Article
Author
Felicio, P.S.; Grasel, R.S.; Campacci, N.; Reis, R.M.; Melendez, M.E.; Palmero, E.I.; de Paula, A.E.; Sabato, C.S.; Fernandes, G.C.; Galvão, H.C.R.; Souza, C.P.; Michelli, R.D.; Andrade, C.E.; Torrezan, G.T.; Barros, B.D.D.F.; Carraro, D.M.; Matsushita, M.M.; Revil, T.; Ragoussis, J.; Tonin, P.N.; Couch, F.J.; Hart, S.N.
Source
In: Human Mutation . (Human Mutation, March 2021, 42(3):290-299)
Subject
Language
English
ISSN
10981004
10597794
10597794