Comment on ‘increased frequency of combined methylenetetrahydrofolate reductase C677T and A1298C mutated alleles in spontaneously aborted embryos’ (multiple letters) [2]

European Journal of Human Genetics

Volumn 10, Issue 10, 2002, Pages 578-582

  Isotalo, Phillip A ^a   Donnelly, James G ^b  

^a MAYO CLINIC   (United States)

^b NEW YORK UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); FOLIC ACID;

DNA DETERMINATION; DNA SEQUENCE; ETHNOLOGY; FETUS DEVELOPMENT; FOLIC ACID DEFICIENCY; GENE FREQUENCY; GENE MUTATION; GENETIC IDENTIFICATION; GENETIC POLYMORPHISM; GENOTYPE; HUMAN; LETTER; MEDICAL LITERATURE; MUTATIONAL ANALYSIS; PRENATAL CARE; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SILENT GENE; SPINA BIFIDA; SPONTANEOUS ABORTION; VITAMIN SUPPLEMENTATION;

ABORTION, SPONTANEOUS; ALLELES; FEMALE; HUMANS; LINKAGE DISEQUILIBRIUM; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); MUTATION; OXIDOREDUCTASES ACTING ON CH-NH GROUP DONORS; POINT MUTATION; PREGNANCY;

EID: 0036801949     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200862     Document Type: Letter

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