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Revil, Timothée

https://orcid.org/0000-0003-1210-7748

A5008283560 | I5023651

Mayo Clinic

McGill University

Citations 1

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

Human Mutation | December 18, 2020 | Volume: 42 | Issue: 3 | Pages: 290-299

10.1002/humu.24158 | PMID 33326660