SEMA3A rs7804122 polymorphism is associated with Hirschsprung disease in the Northeastern region of China

Birth Defects Research Part A - Clinical and Molecular Teratology

Volumn 94, Issue 2, 2012, Pages 91-95

  Wang, Li Li ^a   Zhang, Yi ^a   Fan, Yang ^a   Li, Hui ^a   Zhou, Feng Hua ^a   Miao, Jia Ning ^a   Gu, Hui ^a   Huang, Tian Chu ^a   Yuan, Zheng Wei ^a  

^a CHINA MEDICAL UNIVERSITY   (China)

Author keywords

Association; Hirschsprung disease; Individual susceptibility; Semaphorin 3A; Single nucleotide polymorphism

Indexed keywords

GENOMIC DNA; SEMAPHORIN 3A;

ARTICLE; CHINA; CONTROLLED STUDY; EXON; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENOTYPE; HIRSCHSPRUNG DISEASE; HUMAN; INTRON; MAJOR CLINICAL STUDY; MALE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RNA SPLICING; SINGLE NUCLEOTIDE POLYMORPHISM;

ASIAN CONTINENTAL ANCESTRY GROUP; CHINA; EXONS; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HETEROZYGOTE; HIRSCHSPRUNG DISEASE; HUMANS; INTRONS; MALE; MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; SEMAPHORIN-3A;

EID: 84863075259     PISSN: 15420752     EISSN: 15420760     Source Type: Journal    
DOI: 10.1002/bdra.22866     Document Type: Article

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