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Diagnostic power and clinical impact of exome sequencing in a cohort of 500 patients with rare diseases.
Am J Med Genet C Semin Med Genet. 2020 Dec;184(4):955-964. doi: 10.1002/ajmg.c.31860. Epub 2020 Nov 30.
Am J Med Genet C Semin Med Genet. 2020.
PMID: 33258288
Parental segregation study reveals rare benign and likely benign variants in a Brazilian cohort of rare diseases.
Quaio CRD'C, Ceroni JRM, Cervato MC, Thurow HS, Moreira CM, Trindade ACG, Furuzawa CR, de Souza RRF, Perazzio SF, Dutra AP, Chung CH, Kim CA.
Quaio CRD'C, et al. Among authors: trindade acg.
Sci Rep. 2022 May 11;12(1):7764. doi: 10.1038/s41598-022-11932-z.
Sci Rep. 2022.
PMID: 35546177
Free PMC article.
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Lack of association of GSTT1, GSTM1, GSTO1, GSTP1 and CYP1A1 polymorphisms for susceptibility and outcome in Brazilian prostate cancer patients.
Lima MM Jr, Oliveira MN, Granja F, Trindade AC, De Castro Santos LE, Ward LS.
Lima MM Jr, et al.
Folia Biol (Praha). 2008;54(3):102-8.
Folia Biol (Praha). 2008.
PMID: 18647550
Free article.
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