Studies with His475Tyr glutamate carboxipeptidase II polymorphism and neural tube defects
- 11 June 2002
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 111 (2) , 218-219
- https://doi.org/10.1002/ajmg.10568
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Centre d'Etude du polymorphisme humain (CEPH): Collaborative genetic mapping of the human genomePublished by Elsevier ,2004
- Quantitative effects on gene silencing by allelic variation at a tetranucleotide microsatelliteHuman Molecular Genetics, 2001
- A polymorphic dinucleotide repeat in the rat nucleolin gene forms Z-DNA and inhibits promoter activityProceedings of the National Academy of Sciences, 2001
- Glutamate carboxypeptidase II: a polymorphism associated with lower levels of serum folate and hyperhomocysteinemiaHuman Molecular Genetics, 2000
- DNA polymorphism-diet-cofactor-development hypothesis and the gene-teratogen model for schizophrenia and other developmental disordersAmerican Journal of Medical Genetics, 1999
- Analysis of select folate pathway genes,PAX3, and humanT in a midwestern neural tube defect populationTeratology, 1999
- PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencingNucleic Acids Research, 1997
- 5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defectsAmerican Journal of Medical Genetics, 1996
- Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifidaThe Lancet, 1995