Neural basis of genetically determined visuospatial construction deficit in Williams syndrome

Neuron

Volumn 43, Issue 5, 2004, Pages 623-631

  Meyer Lindenberg, Andreas ^a   Kohn, Philip ^a   Mervis, Carolyn B ^b   Kippenhan, J Shane ^a   Olsen, Rosanna K ^a   Morris, Colleen A ^c   Berman, Karen Faith ^a  

^a NATIONAL INSTITUTE OF MENTAL HEALTH   (United States)

^b UNIVERSITY OF LOUISVILLE   (United States)

^c UNIVERSITY OF NEVADA SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BRAIN REGION; CLINICAL ARTICLE; COGNITIVE DEFECT; CONTROLLED STUDY; FEMALE; GRAY MATTER; HUMAN; MALE; MORPHOMETRICS; NERVE CELL; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; PATH ANALYSIS; PRIORITY JOURNAL; VISION; WILLIAMS BEUREN SYNDROME;

ADULT; ATTENTION; CHROMOSOMES, HUMAN, PAIR 7; FEMALE; FUNCTIONAL LATERALITY; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; MODELS, NEUROLOGICAL; MUTATION; NERVOUS SYSTEM MALFORMATIONS; NEUROPSYCHOLOGICAL TESTS; PARIETAL LOBE; PATTERN RECOGNITION, VISUAL; SPACE PERCEPTION; VISUAL CORTEX; VISUAL PATHWAYS; WILLIAMS SYNDROME;

EID: 4444331998     PISSN: 08966273     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuron.2004.08.014     Document Type: Article

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