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Birth Defects Research. Part A, Clinical and Molecular Teratology|July 20, 2011
MicroRNA gene expression signatures in the developing neural tubePartha Mukhopadhyay, Guy Brock, Savitri Appana, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 20, 2011
A description of congenital anomalies among infants in Entebbe, UgandaJuliet Ndibazza, Swaib Lule, Margaret Nampijja, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 30, 2011
Inclusion and exclusion criteria for malformations in newborn infants exposed to potential teratogensLewis B Holmes, Marie-Noel Westgate
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 29, 2011
Maternal occupational pesticide exposure and risk of hypospadias in the National Birth Defects Prevention StudyCarissa M Rocheleau, Paul A Romitti, Wayne T Sanderson, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 1, 2011
Time trends and geographic variations in the prevalence of hypospadias in ChinaYuehua Li, Meng Mao, Li Dai, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 31, 2012
Hypothesis: terminal transverse limb defects with "nubbins" represent a regenerative process during limb development in human fetusesDavid M Gardiner, Lewis B Holmes
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 19, 2012
Agreement between self-report and prescription data in medical records for pregnant womenPreeyaporn Sarangarm, Bonnie Young, William Rayburn, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 17, 2012
Associated malformations among infants with anophthalmia and microphthalmiaClaude Stoll, Beatrice Dott, Yves Alembik, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 14, 2012
Evidence of gene-environment interaction for the RUNX2 gene and environmental tobacco smoke in controlling the risk of cleft lip with/without cleft palateTao Wu, M Daniele Fallin, Min Shi, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 21, 2011
SEMA3A rs7804122 polymorphism is associated with Hirschsprung disease in the Northeastern region of ChinaLi-Li Wang, Yi Zhang, Yang Fan, et al.
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