Detalhe da pesquisa
1.
Overlapping 16p13.11 deletion and gain of copies variations associated with childhood onset psychosis include genes with mechanistic implications for autism associated pathways: Two case reports.
Am J Med Genet A
; 170A(5): 1165-73, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26887912
2.
Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders.
Am J Med Genet B Neuropsychiatr Genet
; 153B(4): 937-47, 2010 Jun 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-20468056