Detalhe da pesquisa
1.
ELMO2 biallelic pathogenic variants in a patient with gingival hypertrophy and cherubism phenotype: Case report and molecular review.
Am J Med Genet A
; : e63602, 2024 Mar 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38517102
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