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Galvão, Henrique C.R.

https://orcid.org/0000-0002-8017-6537

A5113243402 | I4210093009

Hospital de Câncer de Barretos

Citations 3

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

Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

Human Mutation | May 27, 2019 | Volume: 40 | Issue: 9 | Pages: 1557-1578

10.1002/humu.23818 | PMID 31131967

Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

Human Mutation | February 15, 2018 | Volume: 39 | Issue: 5 | Pages: 593-620

10.1002/humu.23406 | PMID 29446198