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BMC Medical Genetics|July 13, 2006
Analysis of RNA splicing defects in PITX2 mutants supports a gene dosage model of Axenfeld-Rieger syndromeNicole L Maciolek, Wallace L M Alward, Jeffrey C Murray, et al.Health Policy and Planning|March 14, 2009
Prenatal care effectiveness and utilization in BrazilGeorge L Wehby, Jeffrey C Murray, Eduardo E Castilla, et al.Health Economics|January 15, 2009
Quantile effects of prenatal care utilization on birth weight in ArgentinaGeorge L Wehby, Jeffrey C Murray, Eduardo E Castilla, et al.Economics and Human Biology|December 9, 2008
Prenatal care demand and its effects on birth outcomes by birth defect status in ArgentinaGeorge L Wehby, Jeffrey C Murray, Eduardo E Castilla, et al.Journal of Medical Genetics|September 16, 2009
A cohort study of recurrence patterns among more than 54,000 relatives of oral cleft cases in Denmark: support for the multifactorial threshold model of inheritanceDorthe Grosen, Cécile Chevrier, Axel Skytthe, et al.Nature Genetics|December 4, 2001
Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski-/- miceClemencia Colmenares, Heidi A Heilstedt, Lisa G Shaffer, et al.The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|May 8, 2003
Genetic association studies of cleft lip and/or palate with hypodontia outside the cleft regionRebecca L Slayton, Laura Williams, Jeffrey C Murray, et al.American Journal of Medical Genetics. Part A|February 24, 2007
Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesisAlexandre R Vieira, Adriana Modesto, Raquel Meira, et al.Journal of Neonatal-Perinatal Medicine|September 28, 2015
Determining the prevalence of cytomegalovirus infection in a cohort of preterm infantsMitchell M Pitlick, Kristin Orr, Allison M Momany, et al.Molecular Genetics & Genomic Medicine|April 2, 2014
Analysis of PRICKLE1 in human cleft palate and mouse development demonstrates rare and common variants involved in human malformationsTian Yang, Zhonglin Jia, Whitney Bryant-Pike, et al.Pageof 43