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Volumn 57, Issue 5, 2012, Pages 286-293

Association of genetic polymorphisms in the RET-protooncogene and NRG1 with Hirschsprung disease in Thai patients

Author keywords

congenital megacolon; NRG1; RET protooncogene

Indexed keywords

ARTICLE; CHILD; ETHNICITY; FEMALE; GENETIC RISK; GENOTYPE; HIRSCHSPRUNG DISEASE; HUMAN; MAJOR CLINICAL STUDY; MALE; NRG1 GENE; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PROTO ONCOGENE; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SINGLE NUCLEOTIDE POLYMORPHISM; THAILAND;

EID: 84860500776     PISSN: 14345161     EISSN: 1435232X     Source Type: Journal    
DOI: 10.1038/jhg.2012.18     Document Type: Article
Times cited : (40)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.