Decreased proportion of female newborn infants homozygous for the 677 C→T mutation in methylenetetrahydrofolate reductase [3]

American Journal of Medical Genetics

Volumn 83, Issue 2, 1999, Pages 142-143

  Rozen, R ^a   Fraser, F C ^a   Shaw, G ^a  

^a MCGILL UNIVERSITY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2);

CLEFT LIP; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; HUMAN; HYPERHOMOCYSTEINEMIA; LETTER; MALE; MOLECULAR GENETICS; NEURAL TUBE DEFECT; NUCLEIC ACID BASE SUBSTITUTION; PREVALENCE; PRIORITY JOURNAL; SEX RATIO; SPINA BIFIDA;

CLEFT LIP; FEMALE; HOMOZYGOTE; HUMANS; INFANT, NEWBORN; MALE; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); MUTATION; OXIDOREDUCTASES ACTING ON CH-NH GROUP DONORS; SEX DISTRIBUTION; SPINAL DYSRAPHISM;

EID: 0033548679     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990312)83:2<142::AID-AJMG12>3.0.CO;2-Y     Document Type: Letter

References (11)