Autism and genome-wide association studies

Activitas Nervosa Superior Rediviva

Volumn 52, Issue 1, 2010, Pages 28-30

  Celec, Peter ^a   Ostatníková, Daniela ^a  

^a Faculty of Natural Sciences   (Slovakia)

Author keywords

[No Author keywords available]

Indexed keywords

NEUREXIN; NEUROLIGIN; OXYTOCIN RECEPTOR; STEROID HORMONE; TRANSCRIPTION FACTOR;

ARTICLE; ASPERGER SYNDROME; AUTISM; BRAIN DEVELOPMENT; CHINESE; CHROMOSOME 1; CHROMOSOME 12Q; CHROMOSOME 16P; CHROMOSOME 17Q; CHROMOSOME 19P; CHROMOSOME 3Q; CHROMOSOME 5Q; CHROMOSOME 7Q; CHROMOSOME 8P; CHROMOSOME XP; CNTNAP2 GENE; COHORT ANALYSIS; GENE; GENE DELETION; GENE EXPRESSION; GENE FREQUENCY; GENE INSERTION; GENE LOCUS; GENETIC ASSOCIATION; GENETIC HETEROGENEITY; GENETIC POLYMORPHISM; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HERITABILITY; HUMAN; INHERITANCE; LANGUAGE DEVELOPMENT; META ANALYSIS (TOPIC); MOLECULAR PATHOLOGY; MONOGAMY; PATHOGENESIS; POPULATION BASED CASE CONTROL STUDY; PREVALENCE; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM; TRISOMY; UNIPARENTAL DISOMY;

EID: 84865129592     PISSN: 1337933X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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