Found: 1
Select item for more details and to access through your institution.
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:
- Publication type:
- Article