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Birth Defects Research. Part A, Clinical and Molecular Teratology|March 28, 2012
Klippel-Feil syndrome in a boy exposed inadvertently to cyclophosphamide during pregnancy: a case reportBrissia Lazalde, Jesús Grijalva-Flores, Fernando Guerrero-RomeroBirth Defects Research. Part A, Clinical and Molecular Teratology|May 26, 2012
Major, non-chromosomal, birth defects and maternal physical activity: a systematic reviewAudrey L Flak, Ji Yun Tark, Sarah C Tinker, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|September 15, 2015
Role of the planar cell polarity gene Protein tyrosine kinase 7 in neural tube defects in humansMingqin Wang, Patrizia De Marco, Elisa Merello, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|May 19, 2016
Folic acid fortification and prevalences of neural tube defects, orofacial clefts, and gastroschisis in California, 1989 to 2010Wei Yang, Suzan L Carmichael, Gary M ShawBirth Defects Research. Part A, Clinical and Molecular Teratology|June 9, 2016
Acardiac twin pregnancies part II: Fetal risk of chorangioma and sacrococcygeal teratoma predicted by pump/acardiac umbilical vein diametersMartin J C van Gemert, Peter G J Nikkels, K Marieke Paarlberg, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|April 22, 2016
Joint effects of genetic variants and residential proximity to pesticide applications on hypospadias riskSuzan L Carmichael, Wei Yang, Chen Ma, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|December 15, 2015
Variability in a three-generation family with Pierre Robin sequence, acampomelic campomelic dysplasia, and intellectual disability due to a novel ∼1 Mb deletion upstream of SOX9, and including KCNJ2 and KCNJ16Marco Castori, Irene Bottillo, Silvia Morlino, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|December 15, 2015
Cell death and cell proliferation in human spina bifidaLaura Avagliano, Patrizia Doi, Delfina Tosi, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|February 17, 2016
Novel COL4A1 mutation in an infant with severe dysmorphic syndrome with schizencephaly, periventricular calcifications, and cataract resembling congenital infectionRobert Smigiel, Magdalena Cabala, Aleksandra Jakubiak, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|December 4, 2004
Trisomy 8 mosaicism in a patient with heterotaxiaFowzan S Alkuraya, David J HarrisPageof 126