Studies of reduced folate carrier 1 (RFC1) A80G and 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms with neural tube and orofacial cleft defects

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Bibliographic Details
Published inAmerican journal of medical genetics. Part A Vol. 135A; no. 2; pp. 220 - 223
Main Authors Vieira, Alexandre R., Murray, Jeffrey C., Trembath, Dimitri, Orioli, Iêda M., Castilla, Eduardo E., Cooper, Margaret E., Marazita, Mary L., Lennon-Graham, Felicia, Speer, Marcy
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.06.2005
Subjects
Alleles
Cleft Lip - genetics
Cleft Palate - genetics
Family Health
Female
Gene Frequency
Genotype
Humans
Linkage Disequilibrium
Male
Membrane Transport Proteins - genetics
Methylenetetrahydrofolate Reductase (NADPH2) - genetics
Neural Tube Defects - genetics
Pedigree
Point Mutation
Polymorphism, Genetic
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Bibliography:ArticleID:AJMG30705
NIH - No. DE 08559; No. DE 13076; No. NS39818; No. ES11375
ark:/67375/WNG-JJ2W5RPK-N
The March of Dimes Foundation - No. FY02-212
istex:5075D67681D24E301F421DF0A966CF6FDC2D9D73
Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq), Brazil - No. 522059/96-1
Agencia Nacional de Promocion Cientifica y Technologica, Consejo Nacional de Investigaciones Cientificas y Technologicas, Argentina - No. PICT 495
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ISSN:1552-4825
1552-4833
DOI:10.1002/ajmg.a.30705