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American Journal of Medical Genetics

Volumn 100, Issue 1, 2001, Pages 30-36

Genetically determined low maternal serum dopamine β-hydroxylase levels and the etiology of autism spectrum disorders

(5) Robinson, Paula D a Schutz, Chris K b Macciardi, Fabio c White, Bradley N d Holden, Jeanette J A a

a MCMASTER UNIVERSITY (Canada)

b QUEEN S UNIVERSITY (Canada)

c Ongwanada Resource Centre (Canada)

d UNIVERSITY OF TORONTO (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

DOPAMINE; DOPAMINE BETA MONOOXYGENASE; NORADRENALIN;

ADULT; ALLELE; ARTICLE; AUTISM; CLINICAL ARTICLE; CONTROLLED STUDY; DNA FLANKING REGION; DOPAMINE BLOOD LEVEL; ENZYME ACTIVITY; FEMALE; GENE LOCUS; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; INTERPERSONAL COMMUNICATION; MALE; PRIORITY JOURNAL; SOCIAL INTERACTION; STEREOTYPY;

ALLELES; AUTISTIC DISORDER; DNA; DNA MUTATIONAL ANALYSIS; DOPAMINE BETA-HYDROXYLASE; FAMILY; FAMILY HEALTH; GENOTYPE; MUTAGENESIS, INSERTIONAL; SEQUENCE DELETION;

EID: 0035871950 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/ajmg.1187 Document Type: Article

Times cited : (77)

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