Association of Y chromosome haplotypes with autism

Journal of Child Neurology

Volumn 24, Issue 10, 2009, Pages 1258-1261

  Serajee, Fatema J ^a   Huq, A H M Mahbubul ^a,b  

^a WAYNE STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b WAYNE STATE UNIVERSITY   (United States)

Author keywords

Autism; Haplotype; Nucleotide polymorphism; Y chromosome

Indexed keywords

DNA; INITIATION FACTOR 1A; NEUROLIGIN; NEUROLIGIN 4; TRANSDUCIN; TRANSDUCIN BETA LIKE 1 PROTEIN; UNCLASSIFIED DRUG; CARRIER PROTEIN; EIF1AY PROTEIN, HUMAN; INITIATION FACTOR 1; MEMBRANE PROTEIN; NLGN4X PROTEIN, HUMAN; TBL1Y PROTEIN, HUMAN;

ANEUPLOIDY; ARTICLE; AUTISM; CHILD; CONTROLLED STUDY; DNA DETERMINATION; FEMALE; GENETIC ASSOCIATION; GENOTYPE; HAPLOTYPE; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MALE; MONTE CARLO METHOD; PATHOGENESIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; STRUCTURAL CHROMOSOME ABERRATION; Y CHROMOSOME; CASE CONTROL STUDY; CAUCASIAN; COMPUTER SIMULATION; DNA SEQUENCE; GENE FREQUENCY; GENETIC PREDISPOSITION; GENETICS; RISK; UNITED STATES;

AUTISTIC DISORDER; CARRIER PROTEINS; CASE-CONTROL STUDIES; CHROMOSOMES, HUMAN, Y; COMPUTER SIMULATION; EUKARYOTIC INITIATION FACTOR-1; EUROPEAN CONTINENTAL ANCESTRY GROUP; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; MALE; MEMBRANE PROTEINS; MONTE CARLO METHOD; ODDS RATIO; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ANALYSIS, DNA; TRANSDUCIN; UNITED STATES;

EID: 74949096931     PISSN: 08830738     EISSN: 17088283     Source Type: Journal    
DOI: 10.1177/0883073809333530     Document Type: Article

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