Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia

Human Brain Mapping

Volumn 18, Issue 3, 2003, Pages 194-200

  Belton, Emma ^a   Salmond, Claire H ^a   Watkins, Kate E ^b   Vargha Khadem, Faraneh ^a   Gadian, David G ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b MCGILL UNIVERSITY   (Canada)

Author keywords

Bilateral abnormalities; Caudate nucleus; FOXP2; Voxel based morphometry

Indexed keywords

FOXP2 PROTEIN; GENE PRODUCT; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; BRAIN MAPPING; CAUDATE NUCLEUS; CEREBELLUM; CHILD; DYSPRAXIA; FAMILY; FEMALE; FRONTAL CORTEX; GRAY MATTER; HEMISPHERIC DOMINANCE; HUMAN; HUMAN EXPERIMENT; IMAGE ANALYSIS; MALE; MOTOR CORTEX; NORMAL HUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; OROFACIAL DYSPRAXIA; POINT MUTATION; PRIORITY JOURNAL; TEMPORAL LOBE; VERBAL DYSPRAXIA;

ADOLESCENT; APRAXIAS; CAUDATE NUCLEUS; CHILD; FEMALE; FORKHEAD TRANSCRIPTION FACTORS; FUNCTIONAL LATERALITY; HUMANS; IMAGE PROCESSING, COMPUTER-ASSISTED; MAGNETIC RESONANCE IMAGING; MALE; POINT MUTATION; SPEECH DISORDERS; TRANSCRIPTION FACTORS;

EID: 0037341876     PISSN: 10659471     EISSN: None     Source Type: Journal    
DOI: 10.1002/hbm.10093     Document Type: Article

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