Spina Bifida Research Resource: Study design and participant characteristics
Author:
Publisher
Wiley
Subject
Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology and Child Health
Reference39 articles.
1. Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactions;Boyles;Environmental Health Perspect,2006
2. Evidence that the risk of spina bifida is influenced by genetic variation at the NOS3 locus;Brown;Birth Defects Res A Clin Mol Teratol,2004
3. Genetics of common disorders;Carter;Br Med J,1969
4. Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida;Doolin;Am J Hum Genet,2002
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1. Epidemiology and morbidity of spina bifida in Hispanic Americans: a systematic review;BMJ Public Health;2024-06
2. Genome‐wide association studies of structural birth defects: A review and commentary;Birth Defects Research;2019-10-25
3. The Prevalence and Distribution of Spina Bifida in a Single Major Referral Center in Malaysia;Frontiers in Pediatrics;2017-11-09
4. Exon sequencing ofPAX3andT(Brachyury) in cases with spina bifida;Birth Defects Research Part A: Clinical and Molecular Teratology;2013-07
5. Spina bifida subtypes and sub-phenotypes by maternal race/ethnicity in the National Birth Defects Prevention Study;American Journal of Medical Genetics Part A;2011-12-02
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