about
sameAs
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.An investigation to validate the grammar and phonology screening (GAPS) test to identify children with specific language impairmentDCDC2, KIAA0319 and CMIP are associated with reading-related traitsThe regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles.Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing childrenConnecting the CNTNAP2 Networks with Neurodevelopmental Disorders22q13.2q13.32 genomic regions associated with severity of speech delay, developmental delay, and physical features in Phelan-McDermid syndromeWidespread differences in cortex DNA methylation of the "language gene" CNTNAP2 between humans and chimpanzeesDefining the genetic architecture of human developmental language impairment.Towards identification of individual etiologies by resolving genomic and biological conundrums in patients with autism spectrum disorders.Encoding, memory, and transcoding deficits in Childhood Apraxia of Speech.The genetics of reading disabilities: from phenotypes to candidate genesInvestigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQFOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.Talking HeadsNext-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairmentThree treatments for bilingual children with primary language impairment: examining cross-linguistic and cross-domain effectsA study of the role of the FOXP2 and CNTNAP2 genes in persistent developmental stuttering.Genetic insights into the functional elements of language.Associations of prenatal nicotine exposure and the dopamine related genes ANKK1 and DRD2 to verbal language.A common genetic variant in the neurexin superfamily member CNTNAP2 is associated with increased risk for selective mutism and social anxiety-related traitsNeural correlates of childhood language disorder: a systematic review.Language impairment in a case of a complex chromosomal rearrangement with a breakpoint downstream of FOXP2.Heterozygous deletion of the LRFN2 gene is associated with working memory deficits.Disentangling the myriad genomics of complex disorders, specifically focusing on autism, epilepsy, and schizophrenia.Speech-language pathology insights into genetics and neuroscience: beyond surface behaviour.Modification of spectral features by nonhuman primatesGenes and the long and winding road to cortical construction and cognition.The sound of one hand clapping: overdetermination and the pansensory nature of communication.Right hand, left brain: genetic and evolutionary bases of cerebral asymmetries for language and manual action.Haploinsufficiency of CMIP in a girl with autism spectrum disorder and developmental delay due to a de novo deletion on chromosome 16q23.2.Eight further individuals with intellectual disability and epilepsy carrying bi-allelic CNTNAP2 aberrations allow delineation of the mutational and phenotypic spectrum.FOXP2and the Genetic and Developmental Basis of Human LanguageGagueira desenvolvimental persistente familial: perspectivas genéticas
P2860
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P2860
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Recent advances in the genetics of language impairment
@ast
Recent advances in the genetics of language impairment
@en
Recent advances in the genetics of language impairment
@nl
type
label
Recent advances in the genetics of language impairment
@ast
Recent advances in the genetics of language impairment
@en
Recent advances in the genetics of language impairment
@nl
prefLabel
Recent advances in the genetics of language impairment
@ast
Recent advances in the genetics of language impairment
@en
Recent advances in the genetics of language impairment
@nl
P2860
P356
P1433
P1476
Recent advances in the genetics of language impairment
@en
P2093
Anthony P Monaco
P2860
P2888
P356
10.1186/GM127
P407
P577
2010-01-26T00:00:00Z
P5875
P6179
1047214198