Abnormal folate metabolism and mutation in the methylenetetrahydrofolate reductase gene may be maternal risk factors for Down syndrome

Author:

James S Jill1,Pogribna Marta1,Pogribny Igor P1,Melnyk Stepan1,Hine R Jean1,Gibson James B1,Yi Ping1,Tafoya Dixie L1,Swenson David H1,Wilson Vincent L1,Gaylor David W1

Affiliation:

1. From the Food and Drug Administration–National Center for Toxicological Research, the Division of Biochemical Toxicology, Jefferson, AR; the University of Arkansas for Medical Sciences, the Department of Biochemistry and Molecular Biology and the Department of Dietetics and Nutrition, Little Rock; the Arkansas Children's Hospital, the Division of Pediatric Genetics, Little Rock; Trisomy-21 Resear

Publisher

Oxford University Press (OUP)

Subject

Nutrition and Dietetics,Medicine (miscellaneous)

Reference40 articles.

1. Down syndrome (trisomy 21);Epstein,1995

2. The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms;Antofnarakis;Am J Hum Genet,1992

3. Down syndrome genetics: unravelling a multifactorial disorder;Hernandez;Hum Mol Genet,1996

4. DNA demethylation and pericentromeric rearrangements of chromosome 1.;Ji;Mutat Res,1997

5. An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome;Jeanpierre;Hum Mol Genet,1993

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