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Prevalence of BRCA1/BRCA2 mutations in a Brazilian population sample at-risk for hereditary breast cancer and characterization of its genetic ancestry.
Oncotarget. 2016 Dec 6;7(49):80465-80481. doi: 10.18632/oncotarget.12610.
Oncotarget. 2016.
PMID: 27741520
Free PMC article.
Whole-exome sequencing of non-BRCA1/BRCA2 mutation carrier cases at high-risk for hereditary breast/ovarian cancer.
Felicio PS, Grasel RS, Campacci N, de Paula AE, Galvão HCR, Torrezan GT, Sabato CS, Fernandes GC, Souza CP, Michelli RD, Andrade CE, Barros BDF, Matsushita MM, Revil T, Ragoussis J, Couch FJ, Hart SN, Reis RM, Melendez ME, Tonin PN, Carraro DM, Palmero EI.
Felicio PS, et al. Among authors: sabato cs.
Hum Mutat. 2021 Mar;42(3):290-299. doi: 10.1002/humu.24158. Epub 2020 Dec 28.
Hum Mutat. 2021.
PMID: 33326660
Free PMC article.
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TP53 variants of uncertain significance: increasing challenges in variant interpretation and genetic counseling.
Bittar CM, Vieira IA, Sabato CS, Andreis TF, Alemar B, Artigalás O, Galvão HCR, Macedo GS, Palmero EI, Ashton-Prolla P.
Bittar CM, et al. Among authors: sabato cs.
Fam Cancer. 2019 Oct;18(4):451-456. doi: 10.1007/s10689-019-00140-w.
Fam Cancer. 2019.
PMID: 31321604
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