The 19-bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifida in the Irish population-Reference-Cited by-同舟云学术

The 19-bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifida in the Irish population

Published:2007-06-01 Issue:11 Volume:143A Page:1174-1180
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Parle-McDermott Anne,Pangilinan Faith,Mills James L.,Kirke Peadar N.,Gibney Eileen R.,Troendle James,O'Leary Valerie B.,Molloy Anne M.,Conley Mary,Scott John M.,Brody Lawrence C.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference30 articles.

1. Chromosomal organization of the human dihydrofolate reductase genes: dispersion, selective amplification, and a novel form of polymorphism.

2. Neural-Tube Defects

3. 5, 10-Methylenetetrahydrofolate Reductase Gene Variants and Congenital Anomalies: A HuGE Review

4. Methionine Synthase: High-Resolution Mapping of the Human Gene and Evaluation as a Candidate Locus for Neural Tube Defects

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2. A dihydrofolate reductase 2 ( DHFR2 ) variant is associated with risk of neural tube defects in an Irish cohort but not in a United Kingdom cohort;American Journal of Medical Genetics Part A;2021-02-05

3. One-carbon metabolism and folate transporter genes: Do they factor prominently in the genetic etiology of neural tube defects?;Biochimie;2020-06

4. Dihydrofolate Reductase (DHFR) del19bp Polymorphism and Down Syndrome Offspring;Journal of Molecular Neuroscience;2020-05-22

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