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Birth Defects Research. Part A, Clinical and Molecular Teratology|August 6, 2013
Candidate gene association study implicates p63 in the etiology of nonsyndromic bladder-exstrophy-epispadias complexLihong Qi, Mei Wang, Garima Yagnik, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 17, 2013
Factors associated with distance and time traveled to cleft and craniofacial careCynthia H Cassell, Anne Krohmer, Dara D Mendez, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 10, 2013
Rare missense variants in DVL1, one of the human counterparts of the Drosophila dishevelled gene, do not confer increased risk for neural tube defectsElisa Merello, Zoha Kibar, Redouane Allache, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 1, 2013
Periostin downregulation is an early marker of inhibited neonatal murine lung alveolar septationShawn K Ahlfeld, Yong Gao, Jian Wang, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 5, 2013
Is LMNB1 a susceptibility gene for neural tube defects in humans?Alexis Robinson, Darren Partridge, Ashraf Malhas, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 7, 2013
Quantitative assessment of craniofacial morphology in Johanson-Blizzard syndromeCurtis K Deutsch, Tania Hreczko, Lewis B Holmes
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 30, 2012
Maternal tea consumption during early pregnancy and the risk of spina bifidaMahsa M Yazdy, Sarah C Tinker, Allen A Mitchell, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 6, 2013
Maternal genetic polymorphisms of phase II metabolic enzymes and the risk of fetal neural tube defectsLinlin Wang, Lei Jin, Jufen Liu, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 6, 2013
Second study on the recurrence risk of isolated esophageal atresia with or without trachea-esophageal fistula among first-degree relatives: no evidence for increased risk of recurrence of EA/TEF or for malformations of the VATER/VACTERL association spectrumVera Choinitzki, Nadine Zwink, Enrika Bartels, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 6, 2013
Validation of congenital anomaly coding in Canada's administrative databases compared with a congenital anomaly registryAmy Metcalfe, Barbara Sibbald, R Brian Lowry, et al.
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