Showing results (871-880 of 1,255) with videos related to

Sort By:
Pageof 126
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 6, 2013
An Xp21.3p11.4 duplication observed in a boy with intellectual deficiency and speech delay and his asymptomatic motherLingqian Wu, Jing Liu, Weigang Lv, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 30, 2013
A pilot study using residual newborn dried blood spots to assess the potential role of cytomegalovirus and Toxoplasma gondii in the etiology of congenital hydrocephalusRegina M Simeone, Sonja A Rasmussen, Joanne V Mei, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 10, 2014
Highlights from the United States Food and Drug Administration's public workshop on the development of animal models of pregnancy to address medical countermeasures in an "at-risk" population of pregnant women: Influenza as a case studyDenita Williams, Mallikarjuna S Basavarajappa, Sonja A Rasmussen, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 10, 2014
Genetic studies of ANKRD6 as a molecular switch between Wnt signaling pathways in human neural tube defectsRedouane Allache, Mingqin Wang, Patrizia De Marco, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 10, 2014
Promoter methylation and expression of the VANGL2 gene in the myocardium of pediatric patients with tetralogy of fallotYuan Yuan, Yan Gao, Huijun Wang, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 10, 2014
Barriers to care for children with orofacial clefts in North CarolinaCynthia H Cassell, Paula Strassle, Dara D Mendez, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 9, 2014
Heterozygous DLX5 nonsense mutation associated with isolated split-hand/foot malformation with reduced penetrance and variable expressivity in two unrelated familiesAnna Sowińska-Seidler, Magdalena Badura-Stronka, Anna Latos-Bieleńska, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 1, 2013
Maternal folic acid-deficient diet causes congenital malformations in the mouse eyeCarmen Maestro-de-las-Casas, Juliana Pérez-Miguelsanz, Yamila López-Gordillo, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 22, 2013
Racial/ethnic disparities in timing of death during childhood among children with congenital heart defectsWendy N Nembhard, Ping Xu, Mary K Ethen, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|November 1, 2014
Oropharyngeal teratoma, oral duplication, cervical diplomyelia and anencephaly in a 22-week fetus: A review of the craniofacial teratoma syndromeSilvia Morlino, Marco Castori, Francesca Servadei, et al.
Pageof 126