Showing results (561-570 of 1,190) with videos related to

Sort By:
Pageof 119
Birth Defects Research|July 7, 2017
Differences in neural crest sensitivity to ethanol account for the infrequency of anterior segment defects in the eye compared with craniofacial anomalies in a zebrafish model of fetal alcohol syndromeJessica Eason, Antionette L Williams, Bahaar Chawla, et al.
Birth Defects Research|June 17, 2026
Availability of Folic Acid Fortified Corn Masa Products in Selected Areas in the United StatesSharon Bustrak, Juan D Rodriguez, Lorraine F Yeung, et al.
Birth Defects Research|July 8, 2026
Fetal and Obstetric Complications Among Pregnant Women With Congenital Heart Disease in a Georgia Medicaid DatasetCheryl L Raskind-Hood, Travis M Wilson, Shayli Patel, et al.
Birth Defects Research|July 13, 2026
Replicability in EFDT Studies: Implications of Context Dependence for Virtual Control Groups (VCGs)L David Wise, John M DeSesso
Birth Defects Research|August 2, 2026
Maternal and Early Developmental Effects of Perinatal Exposure to Therapeutically Relevant Doses of Common Nonsteroidal Anti-Inflammatory Drugs in RatsSara Tawany Caetano Dos Santos, Reggina Lorena Mellado Castro, Luara Magalhães, et al.
Birth Defects Research|July 25, 2026
Effects of Nimodipine on Neural Tube Development in Early Chick Embryosİhsan Canbek, Emre Atay, Fatma Fırat, et al.
Birth Defects Research|October 12, 2026
Ameliorative Potential of Green and Red Cabbage Extracts Against Teratogenic and Hepatotoxic Effects of Dimenhydrinate in Chick EmbryoNaila Kanwal, Iram Inayat, Muhammad Ali Kanwal, et al.
Birth Defects Research|September 18, 2026
Compound Heterozygous Mutations in FGA Cause Congenital Afibrinogenemia: A Case Report and Literature ReviewLiangliang Liu, Desheng Yuan, Huaxing Zhao, et al.
Birth Defects Research|January 18, 2018
Gene-gene interaction between MSX1 and TP63 in Asian case-parent trios with nonsyndromic cleft lip with or without cleft palateDongjing Liu, Holger Schwender, Mengying Wang, et al.
Birth Defects Research|January 23, 2018
A neuropathological study of novel RTTN gene mutations causing a familial microcephaly with simplified gyral patternSuzanne Chartier, Caroline Alby, Lucile Boutaud, et al.
Pageof 119