Differences in behavioural phenotype between parental deletion and maternal uniparental disomy in Prader-Willi syndrome: An ERP study

Clinical Neurophysiology

Volumn 116, Issue 6, 2005, Pages 1464-1470

  Stauder, Johannes E A ^a   Boer, Harm ^b   Gerits, Rolf H A ^a   Tummers, Anke ^a   Whittington, Joyce ^c   Curfs, Leopold M G ^a,d  

^a MAASTRICHT UNIVERSITY   (Netherlands)

^b Department for Children Young People and Their Families   (United Kingdom)

^c UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^d MAASTRICHT UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Event related potentials; Maternal uniparental disomy; Parental deletion; Prader Willi syndrome; Response inhibition

Indexed keywords

ADULT; ARTICLE; BEHAVIOR GENETICS; CLINICAL ARTICLE; COGNITION; CONTROLLED STUDY; EVENT RELATED POTENTIAL; FEMALE; GENE DELETION; HUMAN; MALE; PHENOTYPE; PRADER WILLI SYNDROME; PRIORITY JOURNAL; PSYCHOPHYSIOLOGY; REACTION TIME; SCORING SYSTEM; TASK PERFORMANCE; UNIPARENTAL DISOMY;

ADULT; ANALYSIS OF VARIANCE; CHROMOSOME DELETION; ELECTROENCEPHALOGRAPHY; EVOKED POTENTIALS; FEMALE; HUMANS; MALE; PHENOTYPE; PHOTIC STIMULATION; PRADER-WILLI SYNDROME; REACTION TIME; TASK PERFORMANCE AND ANALYSIS; UNIPARENTAL DISOMY;

EID: 20544462316     PISSN: 13882457     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.clinph.2005.02.019     Document Type: Article

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