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Volumn 62, Issue 2, 2010, Pages 104-115

Intronic single nucleotide polymorphisms of engrailed homeobox 2 modulate the disease vulnerability of autism in a han chinese population

Author keywords

Autism; Engrailed homeobox 2; Haplotype; Population, Han Chinese; Single nucleotide polymorphisms, intronic

Indexed keywords

ARTICLE; AUTISM; BINDING SITE; CHINESE; CONTROLLED STUDY; DISEASE PREDISPOSITION; FEMALE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC TRANSCRIPTION; HOMEOBOX; HOMEOBOX 2 GENE; HUMAN; INTRON; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; CHI SQUARE DISTRIBUTION; ETHNOLOGY; GENETIC PREDISPOSITION; GENETICS; GENOTYPE; MIDDLE AGED; PROCEDURES; STATISTICAL MODEL;

EID: 77952966410     PISSN: 0302282X     EISSN: None     Source Type: Journal    
DOI: 10.1159/000315441     Document Type: Article
Times cited : (22)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.