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Genetic Basis of Susceptibility to Environmentally Induced Neural Tube Defects.
- Published in:
- Annals of the New York Academy of Sciences, 2000, v. 919, n. 1, p. 261, doi. 10.1111/j.1749-6632.2000.tb06886.x
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- Article
Maternal Alcohol Use in Relation to Selected Birth Defects.
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- American Journal of Epidemiology, 1991, v. 134, n. 7, p. 691
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- Publication type:
- Article
MATERNAL CIGARETTE SMOKING DURING PREGNANCY IN RELATION TO ORAL CLEFTS.
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- American Journal of Epidemiology, 1990, v. 132, n. 5, p. 926, doi. 10.1093/oxfordjournals.aje.a115735
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- Article
AN EPIDEMIOLOGIC STUDY OF CRANIOSYNOSTOSIS: RISK INDICATORS FOR THE OCCURRENCE OF CRANIOSYNOSTOSIS IN COLORADO.
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- American Journal of Epidemiology, 1988, v. 128, n. 2, p. 431, doi. 10.1093/oxfordjournals.aje.a114983
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- Article
FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 24, p. 4879, doi. 10.1093/hmg/ddp444
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- Article
The Effect of Congenital Anomalies on Mortality Risk in White and Black Infants.
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- American Journal of Public Health, 1999, v. 89, n. 6, p. 887, doi. 10.2105/AJPH.89.6.887
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- Article
NEURAL TUBE AND CRANIOFACIAL DEFECTS WITH SPECIAL EMPHASIS ON FOLATE PATHWAY GENES.
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- Critical Reviews in Oral Biology & Medicine, 1998, v. 9, n. 1, p. 38, doi. 10.1177/10454411980090010201
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- Article
Maternal Occupational Exposure to Polycyclic Aromatic Hydrocarbons and Risk of Oral Cleft-Affected Pregnancies.
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- Cleft Palate Craniofacial Journal, 2013, v. 50, n. 3, p. 337, doi. 10.1597/12-104
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- Article
Gene-nutrient interactions: importance of folic acid and vitamin B12 during early embryogenesis.
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- 2008
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- journal article
Gene-nutrient interactions: Importance of folic acid and vitamin B<sub>12</sub> during early embryogenesis.
- Published in:
- Food & Nutrition Bulletin, 2008, v. 29, p. S86, doi. 10.1177/15648265080292S112
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- Publication type:
- Article
A Genetic Signature of Spina Bifida Risk from Pathway-Informed Comprehensive Gene-Variant Analysis.
- Published in:
- PLoS ONE, 2011, v. 6, n. 11, p. 1, doi. 10.1371/journal.pone.0028408
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- Article
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes.
- Published in:
- Nature Genetics, 2002, v. 32, n. 2, p. 285, doi. 10.1038/ng985
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- Article
Maternal reproductive and demographic characteristics as risk factors for hypospadias.
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- Paediatric & Perinatal Epidemiology, 2007, v. 21, n. 3, p. 210, doi. 10.1111/j.1365-3016.2007.00809.x
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- Article
Hypospadias and maternal exposures to cigarette smoke.
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- Paediatric & Perinatal Epidemiology, 2005, v. 19, n. 6, p. 406, doi. 10.1111/j.1365-3016.2005.00680.x
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- Article
THE AUTHORS REPLY.
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- American Journal of Epidemiology, 2009, v. 150, n. 3, p. 324
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- Article
Endothelial Nitric Oxide Synthase (NOS3) Genetic Variants, Maternal Smoking, Vitamin Use, and Risk of Human Orofacial Clefts.
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- American Journal of Epidemiology, 2005, v. 162, n. 12, p. 1207, doi. 10.1093/aje/kwi336
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- Article
Genetic Variation of Infant Reduced Folate Carrier (A80G) and Risk of Orofacial and Conotruncal Heart Defects.
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- American Journal of Epidemiology, 2003, v. 158, n. 8, p. 747, doi. 10.1093/aje/kwg189
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- Article
Maternal Occupational Chemical Exposures and Biotransformation Genotypes as Risk Factors for Selected Congenital Anomalies.
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- American Journal of Epidemiology, 2003, v. 157, n. 6, p. 475, doi. 10.1093/aje/kwg013
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- Publication type:
- Article
Maternal Vitamin Use, Genetic Variation of Infant Methylenetetrahydrofolate Reducatase, and Risk for spina Bifida.
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- American Journal of Epidemiology, 1998, v. 148, n. 1, p. 30, doi. 10.1093/oxfordjournals.aje.a009555
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- Publication type:
- Article
Maternal Smoking During Early Pregnancy, GSTP1 and EPHX1 Variants, and Risk of Isolated Orofacial Clefts.
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- Cleft Palate Craniofacial Journal, 2007, v. 44, n. 4, p. 366, doi. 10.1597/06-011.1
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- Publication type:
- Article
Lacrimoauriculodentodigital Syndrome With Cleft Lip/Palate and Renal Manifestations.
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- Cleft Palate Craniofacial Journal, 2004, v. 41, n. 5, p. 501, doi. 10.1597/03-080.1
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- Publication type:
- Article
CHKA and PCYT1A gene polymorphisms, choline intake and spina bifida risk in a California population.
- Published in:
- BMC Medicine, 2006, v. 4, p. 1, doi. 10.1186/1741-7015-4-36
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- Publication type:
- Article
Genes encoding critical transcriptional activators for murine neural tube development and human spina bifida: a case-control study.
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- BMC Medical Genetics, 2010, v. 11, p. 141, doi. 10.1186/1471-2350-11-141
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- Article
Association between CFL1 gene polymorphisms and spina bifida risk in a California population.
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- BMC Medical Genetics, 2007, v. 8, p. 1, doi. 10.1186/1471-2350-8-12
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- Publication type:
- Article
Embryonic development of folate binding protein?1 (Folbp1) knockout mice: Effects of the chemical form, dose, and timing of maternal folate supplementation.
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- Developmental Dynamics, 2004, v. 231, n. 1, p. 221
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- Publication type:
- Article
Genetic variation of FOXE1 and risk for orofacial clefts in a California population.
- Published in:
- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 11, p. 2770, doi. 10.1002/ajmg.a.37871
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- Article
Sequence variation in folate pathway genes and risks of human cleft lip with or without cleft palate.
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- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 11, p. 2777, doi. 10.1002/ajmg.a.37874
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- Article
Gene variants as risk factors for gastroschisis.
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- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 11, p. 2788, doi. 10.1002/ajmg.a.37883
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- Article
Identification of novel candidate gene loci and increased sex chromosome aneuploidy among infants with conotruncal heart defects.
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- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 2, p. 397, doi. 10.1002/ajmg.a.36291
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- Article
Considering the vascular hypothesis for the pathogenesis of small intestinal atresia: A case control study of genetic factors.
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- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 4, p. 702, doi. 10.1002/ajmg.a.35775
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- Article
Maternal and infant gene-folate interactions and the risk of neural tube defects.
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- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 10, p. 2439, doi. 10.1002/ajmg.a.35552
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- Article
Thymidylate synthase polymorphisms and risk of conotruncal heart defects.
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- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 9, p. 2194, doi. 10.1002/ajmg.a.35310
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- Publication type:
- Article
Gene variants in the folate-mediated one-carbon metabolism (FOCM) pathway as risk factors for conotruncal heart defects.
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- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 5, p. 1124, doi. 10.1002/ajmg.a.35313
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- Article
De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects.
- Published in:
- PLoS Genetics, 2016, v. 12, n. 4, p. 1, doi. 10.1371/journal.pgen.1005963
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- Article
Haploinsufficiency of insulin gene enhancer protein 1 ( ISL1) is associated with d-transposition of the great arteries.
- Published in:
- Molecular Genetics & Genomic Medicine, 2014, v. 2, n. 4, p. 341, doi. 10.1002/mgg3.75
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- Article
Molecular Characterization of Breakpoints in Patients with Holoprosencephaly and Definition of the HPE2 Critical Region 2p21.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 2, p. 223, doi. 10.1093/hmg/5.2.223
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- Article
Classification and Analysis of Fetal Deaths in Massachusetts.
- Published in:
- JAMA: Journal of the American Medical Association, 1989, v. 261, n. 12, p. 1757, doi. 10.1001/jama.1989.03420120095033
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- Article