Detalhe da pesquisa
1.
The Brazilian Rare Genomes Project: Validation of Whole Genome Sequencing for Rare Diseases Diagnosis.
Front Mol Biosci
; 9: 821582, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35586190
2.
Genomic study of nonsyndromic hearing loss in unaffected individuals: Frequency of pathogenic and likely pathogenic variants in a Brazilian cohort of 2,097 genomes.
Front Genet
; 13: 921324, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36147510
3.
Mass molecular testing for COVID19 using NGS-based technology and a highly scalable workflow.
Sci Rep
; 11(1): 7122, 2021 03 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33782491