Endophenotypes of FOXP2: dysfunction within the human articulatory network.
about
Human brain evolution: from gene discovery to phenotype discoveryFrontal-thalamic circuits associated with languageDopamine regulation of human speech and bird song: a critical review.Neural Correlates of Developmental Speech and Language Disorders: Evidence from NeuroimagingEarly neuroimaging markers of FOXP2 intragenic deletion.Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language DevelopmentGenetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech.Insights into the Neural and Genetic Basis of Vocal Communication.Structural brain abnormalities in a single gene disorder associated with epilepsy, language impairment and intellectual disability.Speech-Sound Disorders and Attention-Deficit/Hyperactivity Disorder Symptoms.Speech-language pathology insights into genetics and neuroscience: beyond surface behaviour.Insights into the genetic foundations of human communication.A Diagnostic Marker to Discriminate Childhood Apraxia of Speech From Speech Delay: I. Development and Description of the Pause Marker.The Neural Basis of Vocal Pitch Imitation in Humans.Frontotemporal dementia and language networks: cortical thickness reduction is driven by dyslexia susceptibility genes.Phonological working memory and FOXP2.Abnormal functional connectivity strength in patients with adolescent-onset schizophrenia: a resting-state fMRI study.Sequential processing deficit as a shared persisting biomarker in dyslexia and childhood apraxia of speech.Global and Local Connectivity Differences Converge With Gene Expression in a Neurodevelopmental Disorder of Known Genetic Origin.Mapping of Human FOXP2 Enhancers Reveals Complex Regulation.FOXP1mutations cause intellectual disability and a recognizable phenotype
P2860
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P2860
Endophenotypes of FOXP2: dysfunction within the human articulatory network.
description
2011 nî lūn-bûn
@nan
2011 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Endophenotypes of FOXP2: dysfunction within the human articulatory network.
@ast
Endophenotypes of FOXP2: dysfunction within the human articulatory network.
@en
type
label
Endophenotypes of FOXP2: dysfunction within the human articulatory network.
@ast
Endophenotypes of FOXP2: dysfunction within the human articulatory network.
@en
prefLabel
Endophenotypes of FOXP2: dysfunction within the human articulatory network.
@ast
Endophenotypes of FOXP2: dysfunction within the human articulatory network.
@en
P2093
P3181
P1476
Endophenotypes of FOXP2: dysfunction within the human articulatory network.
@en
P2093
A Connelly
A T Morgan
F Liégeois
P304
P3181
P356
10.1016/J.EJPN.2011.04.006
P577
2011-05-14T00:00:00Z