Detalhe da pesquisa
1.
Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.
PLoS Genet
; 11(3): e1004925, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25781923
2.
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.
Dev Med Child Neurol
; 56(4): 346-53, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24117048
3.
Correction: Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment.
PLoS Genet
; 11(6): e1005336, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26114769
4.
Genome-wide analysis identifies a role for common copy number variants in specific language impairment.
Eur J Hum Genet
; 23(10): 1370-7, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25585696
5.
Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment.
Eur J Hum Genet
; 22(10): 1165-71, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24518835
6.
Associations of HLA alleles with specific language impairment.
J Neurodev Disord
; 6(1): 1, 2014 Jan 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-24433325
7.
Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'.
Eur J Hum Genet
; 23(9): 1113-5, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25537359