Detalhe da pesquisa
1.
Variants in GNAI1 cause a syndrome associated with variable features including developmental delay, seizures, and hypotonia.
Genet Med
; 23(5): 881-887, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33473207
2.
Family communication in a population at risk for hypertrophic cardiomyopathy.
J Genet Couns
; 24(2): 336-48, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25304619
3.
Quality of life and autonomy in emerging adults with early-onset neuromuscular disorders.
J Genet Couns
; 21(5): 713-25, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22367485