Infant C677T mutation in MTHFR, maternal periconceptional vitamin use, and risk of nonsyndromic cleft lip? [2]

American Journal of Medical Genetics

Volumn 92, Issue 1, 2000, Pages 79-80

  Wyszynski, Diego F ^a,b,c   Diehl, Scott R ^b  

^a BOSTON UNIVERSITY   (United States)

^b NATIONAL INSTITUTE OF DENTAL AND CRANIOFACIAL RESEARCH   (United States)

^c BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

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

BIRTH DEFECT; CASE CONTROL STUDY; CLEFT LIP; CONTROLLED STUDY; GENE MUTATION; GENOTYPE; HUMAN; INFANT; LETTER; LIP MALFORMATION; MAJOR CLINICAL STUDY; PREGNANCY; PRIORITY JOURNAL; VITAMIN INTAKE;

AMINE OXIDOREDUCTASES; CLEFT LIP; FEMALE; HUMAN; INFANT, NEWBORN; POINT MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; PREGNANCY; RISK FACTORS; VITAMINS;

EID: 0034193698     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(20000501)92:1<79::AID-AJMG14>3.0.CO;2-H     Document Type: Letter

References (15)