Dorsal and ventral stream mediated visual processing in genetic subtypes of Prader-Willi syndrome

Neuropsychologia

Volumn 47, Issue 12, 2009, Pages 2367-2373

  Woodcock, Kate A ^a   Humphreys, Glyn W ^a   Oliver, Chris ^a  

^a UNIVERSITY OF BIRMINGHAM   (United Kingdom)

Author keywords

Chromosome 15; Dorsal stream deficit; Dorsal stream vulnerability; Fragile X syndrome; Paternal deletion; Uniparental disomy

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CHILD DEVELOPMENT; CLINICAL ARTICLE; CONTROLLED STUDY; DISOMY; FEMALE; FRAGILE X SYNDROME; GENE DELETION; HUMAN; INTELLECTUAL IMPAIRMENT; INTELLIGENCE QUOTIENT; MALE; PRADER WILLI SYNDROME; TASK PERFORMANCE; VISUAL SYSTEM FUNCTION;

ADOLESCENT; ANALYSIS OF VARIANCE; CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 15; FEMALE; FRAGILE X MENTAL RETARDATION PROTEIN; HUMANS; MALE; NEUROPSYCHOLOGICAL TESTS; PATTERN RECOGNITION, VISUAL; PHOTIC STIMULATION; PRADER-WILLI SYNDROME; PROBLEM SOLVING; REACTION TIME; SPACE PERCEPTION; VISUAL PATHWAYS; YOUNG ADULT;

EID: 67650064623     PISSN: 00283932     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuropsychologia.2008.09.019     Document Type: Article

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