Detalhe da pesquisa
1.
Phenotypic heterogeneity in 22q11.2 deletion syndrome: Copy Number Variants as genetic modifiers for congenital heart disease in a Brazilian cohort.
Am J Med Genet A
; 191(5): 1273-1281, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36751694