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Birth Defects Research. Part A, Clinical and Molecular Teratology|August 1, 2009
Pena-Shokeir phenotype (fetal akinesia deformation sequence) revisitedJudith G Hall
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 24, 2009
Public health projects for preventing the recurrence of neural tube defects in the United StatesJulianne S Collins, Mark A Canfield, Kay Pearson, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 29, 2009
Women's perspectives on counseling about risks for medication-induced birth defectsAimee K Santucci, Melanie A Gold, Aletha Y Akers, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 28, 2009
Maternal caffeine consumption and risk of neural tube defectsRebecca J Schmidt, Paul A Romitti, Trudy L Burns, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 25, 2009
False positive reporting of Hirschsprung's disease in Alaska: an evaluation of Hirschsprung's disease surveillance, birth years 1996-2007Janine Schoellhorn, Sandra Collins
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 18, 2009
Epidemiologic features and clinical subgroups of anotia/microtia in TexasMark A Canfield, Peter H Langlois, Ly M Nguyen, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 19, 2009
Association of congenital cardiovascular malformations with 33 single nucleotide polymorphisms of selected cardiovascular disease-related genesKaren Kuehl, Christopher Loffredo, Edward J Lammer, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 15, 2010
The relationship between sonic Hedgehog signaling, cilia, and neural tube defectsJennifer N Murdoch, Andrew J Copp
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 22, 2008
Characteristics of a spina bifida population including North American Caucasian and Hispanic individualsKit Sing Au, Phong X Tran, Chester C Tsai, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 28, 2012
Rare case of XX/XY mosaicism and trisomy 13 in early prenatal diagnosisStavros Sifakis, Katherine Anagnostopoulou, Konstantina Plastira, et al.
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