Detalhe da pesquisa
1.
Mutations in SOX2 cause anophthalmia.
Nat Genet
; 33(4): 461-3, 2003 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-12612584
2.
Peripatetic southern cytogenetics.
Genet Med
; 17(5): 425-6, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25356973
3.
The course of cognitive-behavioral development in children with the FMR1 mutation, Williams-Beuren syndrome, and neurofibromatosis type 1: The effect of gender.
Am J Med Genet A
; 152A(6): 1498-509, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20503326
4.
Developmental trajectories in syndromes with intellectual disability, with a focus on Wolf-Hirschhorn and its cognitive-behavioral profile.
Am J Intellect Dev Disabil
; 117(2): 167-79, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22515830
5.
Studies of age-correlated features of cognitive-behavioral development in children and adolescents with genetic disorders.
Am J Med Genet A
; 143A(20): 2478-89, 2007 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17853466