Detalhe da pesquisa
1.
Whole-exome sequencing of non-BRCA1/BRCA2 mutation carrier cases at high-risk for hereditary breast/ovarian cancer.
Hum Mutat
; 42(3): 290-299, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33326660
2.
Oncogenetics service and the Brazilian public health system: the experience of a reference Cancer Hospital.
Genet Mol Biol
; 39(2): 168-77, 2016 May 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-27192127
3.
XAF1 as a modifier of p53 function and cancer susceptibility.
Sci Adv
; 6(26): eaba3231, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32637605
4.
Genotype and phenotype landscape of MEN2 in 554 medullary thyroid cancer patients: the BrasMEN study.
Endocr Connect
; 8(3): 289-298, 2019 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30763276
5.
Genetic alterations detected by comparative genomic hybridization in BRCAX breast and ovarian cancers of Brazilian population.
Oncotarget
; 9(44): 27525-27534, 2018 Jun 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29938003
6.
Prevalence of BRCA1/BRCA2 mutations in a Brazilian population sample at-risk for hereditary breast cancer and characterization of its genetic ancestry.
Oncotarget
; 7(49): 80465-80481, 2016 Dec 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27741520