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Birth Defects Research. Part A, Clinical and Molecular Teratology|March 13, 2016
Compound heterozygosity of a paternal submicroscopic deletion and a maternal missense mutation in POR gene: Antley-bixler syndrome phenotype in three sibling fetusesMaria Tzetis, Anastasia Konstantinidou, Christalena Sofocleous, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 29, 2015
Evaluating cost and resource use associated with pulse oximetry screening for critical congenital heart disease: Empiric estimates and sources of variationMatthew R Reeder, Jaewhan Kim, Amy Nance, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 12, 2016
Levels of folate receptor autoantibodies in maternal and cord blood and risk of neural tube defects in a Chinese populationNa Yang, Linlin Wang, Richard H Finnell, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 14, 2016
Determining the association between methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms and genomic DNA methylation level: A meta-analysisLi Wang, Shaofang Shangguan, Shaoyan Chang, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 15, 2016
Prenatal diagnosis, hospital characteristics, and mortality in transposition of the great arteriesDiego A Lara, David E Fixler, Mary K Ethen, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 16, 2016
Is advanced maternal age a risk factor for congenital heart disease?Kate E Best, Judith Rankin
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 16, 2016
Management and outcomes of neonates with down syndrome admitted to neonatal unitsJake P Mann, Eugene Statnikov, Neena Modi, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 16, 2016
Evidence for a teratogenic risk in the offspring of health personnel exposed to ionizing radiation?!Awi Wiesel, Gabriela Stolz, Annette Queisser-Wahrendorf
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 28, 2016
A novel 2q14.1q14.3 deletion involving GLI2 and RNU4ATAC genes associated with partial corpus callosum agenesis and severe intrauterine growth retardationCarole Goumy, Mathilde Gay-Bellile, Gaelle Salaun, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 7, 2016
AGORA, a data- and biobank for birth defects and childhood cancerIris A L M van Rooij, Loes F M van der Zanden, Ernie M H F Bongers, et al.
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