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Birth Defects Research. Part A, Clinical and Molecular Teratology|January 17, 2012
Abnormal WT1 expression in human fetuses with bilateral renal agenesis and cardiac malformationsChristine K C Loo, Tamara N Pereira, Grant A Ramm
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 17, 2012
Periconceptional folic acid use: still room to improvePriscilla A Zetstra-van der Woude, Hermien E K de Walle, Lolkje T W de Jong-van den Berg
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 19, 2012
Working towards a risk prediction model for neural tube defectsA J Agopian, Philip J Lupo, Sarah C Tinker, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 4, 2011
Getting to the heart of planar cell polarity signalingDeborah J Henderson, Bill Chaudhry
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 4, 2011
Xenopus: An emerging model for studying congenital heart diseaseErin Kaltenbrun, Panna Tandon, Nirav M Amin, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 4, 2011
TGFβ signaling and congenital heart disease: Insights from mouse studiesHelen M Arthur, Simon D Bamforth
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 4, 2011
Facial suture synostosis of newborn Fgfr1(P250R/+) and Fgfr2(S252W/+) mouse models of Pfeiffer and Apert syndromesRoopa Purushothaman, Timothy C Cox, A Murat Maga, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 4, 2011
A double abdominal aorta with a double inferior vena cava: a human congenital vascular patterning defectArda Kayhan, Jack Collins, Jafar Al-Sadir, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 2, 2011
Origin and development of the atrioventricular myocardial lineage: insight into the development of accessory pathwaysWim T J Aanhaanen, Antoon F M Moorman, Vincent M Christoffels
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 9, 2011
Paper 5: Surveillance of multiple congenital anomalies: implementation of a computer algorithm in European registers for classification of casesEster Garne, Helen Dolk, Maria Loane, et al.
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