New 19 bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR): A risk factor for spina bifida acting in mothers during pregnancy?
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.20505/fullpdf
Reference52 articles.
1. Investigation of Folate Pathway Gene Polymorphisms and the Incidence of Neural Tube Defects in a Texas Hispanic Population
2. Elevated plasma total homocysteine and C677T mutation of the methylenetetrahydrofolate reductase gene in patients with spina bifida
3. 677right-arrowCT mutation on the methylenetetrahydrofolate reductase gene is not a risk factor for neural tube defects in Turkey
4. Parental sex effect in spina bifida: A role for genomic imprinting?
5. The functional human dihydrofolate reductase gene.
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