TPH2 G/T polymorphism is associated with hyperphagia, IQ, and internalizing problems in Prader-Willi syndrome

Journal of Child Psychology and Psychiatry and Allied Disciplines

Volumn 52, Issue 5, 2011, Pages 580-587

  Dykens, Elisabeth M ^a   Roof, Elizabeth ^a   Bittel, Douglas ^b   Butler, Merlin G ^c  

^a VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

^b UNIVERSITY OF MISSOURI KANSAS CITY SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF KANSAS MEDICAL CENTER   (United States)

Author keywords

Behavior problems; genetics; intelligence; internalizing disorder; neurochemistry; Prader Willi syndrome

Indexed keywords

TPH2 PROTEIN, HUMAN; TRYPTOPHAN HYDROXYLASE;

ADOLESCENT; ADULT; ARTICLE; CHILD; CONTROL; FEMALE; GENETICS; GENOTYPE; HUMAN; HYPERPHAGIA; INTELLIGENCE; MALE; MIDDLE AGED; MOTHER; PHENOTYPE; PRADER WILLI SYNDROME; PRESCHOOL CHILD; PSYCHOLOGICAL ASPECT; QUESTIONNAIRE; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; FEMALE; GENOTYPE; HUMANS; HYPERPHAGIA; INTELLIGENCE; INTERNAL-EXTERNAL CONTROL; MALE; MIDDLE AGED; MOTHERS; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; PRADER-WILLI SYNDROME; QUESTIONNAIRES; TRYPTOPHAN HYDROXYLASE; YOUNG ADULT;

EID: 79954895397     PISSN: 00219630     EISSN: 14697610     Source Type: Journal    
DOI: 10.1111/j.1469-7610.2011.02365.x     Document Type: Article

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