Discovery of allelic variants of HOXA1 and HOXB1: Genetic susceptibility to autism spectrum disorders

Teratology

Volumn 62, Issue 6, 2000, Pages 393-405

  Ingram, Jennifer L ^a   Stodgell, Christopher J ^a   Hyman, Susan L ^a   Figlewicz, Denise A ^a   Weitkamp, Lowell R ^a   Rodier, Patricia M ^a  

^a UNIVERSITY OF ROCHESTER SCHOOL OF MEDICINE AND DENTISTRY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; HOXA1 PROTEIN; HOXB1 PROTEIN; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; AUTISM; BRAIN STEM INJURY; DNA SEQUENCE; FEMALE; GENE INSERTION; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; RISK FACTOR; SEQUENCE ANALYSIS;

ABNORMALITIES, MULTIPLE; ALLELES; ASPERGER SYNDROME; AUTISTIC DISORDER; BRAIN STEM; COMORBIDITY; DNA MUTATIONAL ANALYSIS; EMBRYONIC AND FETAL DEVELOPMENT; ETHNIC GROUPS; FEMALE; GENES, HOMEOBOX; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HOMEODOMAIN PROTEINS; HUMANS; MALE; MENTAL RETARDATION; NEW YORK; PHENOTYPE; POINT MUTATION; POLYMERASE CHAIN REACTION; TRANSCRIPTION FACTORS;

MAMMALIA;

EID: 0033667613     PISSN: 00403709     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-9926(200012)62:6<393::AID-TERA6>3.0.CO;2-V     Document Type: Article

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