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Birth Defects Research. Part A, Clinical and Molecular Teratology|December 1, 2007
Craniosynostosis and maternal smokingSuzan L Carmichael, Chen Ma, Sonja A Rasmussen, et al.
American Journal of Medical Genetics. Part A|October 16, 2013
Identification of novel candidate gene loci and increased sex chromosome aneuploidy among infants with conotruncal heart defectsKazutoyo Osoegawa, David M Iovannisci, Bin Lin, et al.
Molecular Genetics and Metabolism|November 1, 2005
A known functional polymorphism (Ile120Val) of the human PCMT1 gene and risk of spina bifidaHuiping Zhu, Wei Yang, Wei Lu, et al.
Clinical Radiology|March 18, 2014
Diagnostic workup of primary sclerosing cholangitis: the benefit of adding gadoxetic acid-enhanced T1-weighted magnetic resonance cholangiography to conventional T2-weighted magnetic resonance cholangiographyR Nolz, U Asenbaum, M Schoder, et al.
American Journal of Medical Genetics. Part A|January 27, 2010
Planar cell polarity pathway genes and risk for spina bifidaShu Wen, Huiping Zhu, Wei Lu, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|February 14, 2013
Thymidylate synthase polymorphisms and risks of human orofacial cleftsGary M Shaw, Wei Yang, Spencer Perloff, et al.
The Annals of Thoracic Surgery|March 29, 2000
Thoracic aortic aneurysms: treatment with endovascular self-expandable stent graftsM Grabenwöger, D Hutschala, M P Ehrlich, et al.
American Journal of Medical Genetics|July 27, 2001
Analysis of the EPHX1 113 polymorphism and GSTM1 homozygous null polymorphism and oral clefting associated with maternal smokingJ K Hartsfield, T A Hickman, E T Everett, et al.
Teratology|November 1, 1990
Sensitivity, specificity, and positive predictive value of multiple malformations in isotretinoin embryopathy surveillanceM C Lynberg, M J Khoury, E J Lammer, et al.
Toxicology and Applied Pharmacology|July 9, 2004
Gene-nutrient interactions: importance of folates and retinoids during early embryogenesisRichard H Finnell, Gary M Shaw, Edward J Lammer, et al.
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