Detalhe da pesquisa
1.
Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556.
Neurogenetics
; 20(2): 91-98, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30982090