Further evidence from haplotype analysis for linkage of the dopamine D4 receptor gene and attention-deficit hyperactivity disorder

American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 96, Issue 3, 2000, Pages 262-267

  Barr, Cathy L ^a,b   Wigg, Karen G ^a   Bloom, Stacey ^b   Schachar, Russell ^b   Tannock, Rosemary ^b   Roberts, Wendy ^b   Malone, Molly ^b   Kennedy, James L ^c  

^a TORONTO WESTERN HOSPITAL   (Canada)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

^c UNIVERSITY OF TORONTO   (Canada)

Author keywords

Attention deficit hyperactivity disorder; Dopamine receptor D4; Genetics; Haplotypes; Transmission Disequilibrium Test; Tyrosine hydroxylase

Indexed keywords

DOPAMINE 4 RECEPTOR; TYROSINE 3 MONOOXYGENASE;

ALLELE; ARTICLE; ATTENTION DEFICIT DISORDER; EXON; GENE DELETION; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC LINKAGE; GENETIC POLYMORPHISM; HAPLOTYPE; HUMAN; HUMAN CELL; PRIORITY JOURNAL;

ADOLESCENT; ALLELES; ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; CHI-SQUARE DISTRIBUTION; CHILD; FAMILY HEALTH; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; RECEPTORS, DOPAMINE D2; RECEPTORS, DOPAMINE D4; STATISTICS; TYROSINE 3-MONOOXYGENASE;

EID: 0034640717     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/1096-8628(20000612)96:3<262::AID-AJMG5>3.0.CO;2-8     Document Type: Article

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