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Volumn 67, Issue 4, 2000, Pages 986-990

Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: An examination of C677T and A1298C mutations

(3) Isotalo, Phillip A a Wells, George A a,b Donnelly, James G a,c

a UNIVERSITY OF OTTAWA (Canada)

b Loeb Med Res Inst London H (Canada)

c UNIVERSITY OF OTTAWA (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2);

ARTICLE; CONTROLLED STUDY; FETUS DEVELOPMENT; GENE MUTATION; GENETIC POLYMORPHISM; GENOTYPE; HUMAN; HYPERHOMOCYSTEINEMIA; MAJOR CLINICAL STUDY; NEURAL TUBE DEFECT; NEWBORN; PRIORITY JOURNAL; RISK FACTOR;

EID: 0033794925 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: 10.1086/303082 Document Type: Article

Times cited : (192)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.