Detalhe da pesquisa
1.
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Nat Genet
; 39(3): 319-28, 2007 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-17322880
2.
Rare deletions at the neurexin 3 locus in autism spectrum disorder.
Am J Hum Genet
; 90(1): 133-41, 2012 Jan 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-22209245
3.
Concordance of Diagnosis of Autism Spectrum Disorder Made by Pediatricians vs a Multidisciplinary Specialist Team.
JAMA Netw Open
; 6(1): e2252879, 2023 01 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36696109
4.
Understanding the Use of the Term "Weaponized Autism" in An Alt-Right Social Media Platform.
J Autism Dev Disord
; 53(10): 4035-4046, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-35947316
5.
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
Nat Neurosci
; 20(4): 602-611, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-28263302
6.
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability.
Sci Transl Med
; 2(49): 49ra68, 2010 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20844286
7.
Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2.
Am J Med Genet A
; 140(5): 509-14, 2006 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-16470794
8.
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia.
Am J Hum Genet
; 79(5): 965-72, 2006 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17033973
9.
Executive processes in appearance-reality tasks: the role of inhibition of attention and symbolic representation.
Child Dev
; 75(2): 562-79, 2004.
Artigo
em Inglês
| MEDLINE | ID: mdl-15056206