Detalhe da pesquisa
1.
A novel 2q37 microdeletion containing human neural progenitors genes including STK25 results in severe developmental delay, epilepsy, and microcephaly.
Am J Med Genet A
; 167A(11): 2808-16, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26238961