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Birth Defects Research. Part A, Clinical and Molecular Teratology|October 12, 2011
Is gastroschisis truly a sporadic defect?: familial cases of gastroschisis in Utah, 1997 to 2008Marcia L Feldkamp, John C Carey, Richard Pimentel, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|February 29, 2012
Spectrum of congenital anomalies in pregnancies with pregestational diabetesEster Garne, Maria Loane, Helen Dolk, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|February 29, 2012
Is maternal parity an independent risk factor for birth defects?Hao T Duong, Adrienne T Hoyt, Suzan L Carmichael, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 2, 2011
Functional analyses of RET mutations in Chinese Hirschsprung disease patientsThomas Y Y Leon, Man-Ting So, Vincent C H Lui, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 28, 2012
Using ICD-9 codes to establish prevalence of malformations in newborn infantsLewis B Holmes, Marie-Noel Westgate
Birth Defects Research. Part A, Clinical and Molecular Teratology|February 8, 2006
Mutational screening of the CYP26A1 gene in patients with caudal regression syndromePatrizia De Marco, Elisa Merello, Samantha Mascelli, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|February 8, 2006
Cleidocranial dysplasia with severe parietal bone dysplasia: C-terminal RUNX2 mutationsMichael L Cunningham, Marianne L Seto, Anne V Hing, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|November 30, 2007
Nonlinear imaging study of extracellular matrix in chemical-induced, developmental dissecting aortic aneurysm: evidence for defective collagen type IIIBin Gong, Ju Sun, Grace Vargas, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|November 30, 2007
Birth defects in uncles and aunts from Irish families with neural tube defectsJulianne Byrne
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 31, 2008
Interindividual variability in acetaminophen sulfation by human fetal liver: implications for pharmacogenetic investigations of drug-induced birth defectsAraba A Adjei, Andrea Gaedigk, Stephen D Simon, et al.
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