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The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|June 24, 2021
Academic Achievement Among Children With Nonsyndromic Orofacial Clefts : A Population-Based StudyStephanie E Watkins, Robert E Meyer, Arthur S Aylsworth, et al.American Journal of Perinatology|February 23, 2010
Deletion of hepatocyte nuclear factor-1-beta in an infant with prune belly syndromeSina Haeri, Patricia L Devers, Kathleen A Kaiser-Rogers, et al.European Journal of Human Genetics : EJHG|February 10, 2012
Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypesJill A Rosenfeld, Ryan N Traylor, G Bradley Schaefer, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|August 8, 2015
Issues involved in the phenotypic classification of orofacial clefts ascertained through a state birth defects registry for the North Carolina Cleft Outcomes StudyArthur S Aylsworth, Alexander C Allori, Luiz A Pimenta, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 18, 2007
The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndromeLisa G Shaffer, Aaron Theisen, Bassem A Bejjani, et al.The Journal of Molecular Diagnostics : JMD|April 29, 2006
Diagnosis of human congenital cytomegalovirus infection by amplification of viral DNA from dried blood spots on perinatal cardsLori Scanga, Shu Chaing, Cynthia Powell, et al.American Journal of Medical Genetics. Part A|December 15, 2015
Survival of children with trisomy 13 and trisomy 18: A multi-state population-based studyRobert E Meyer, Gang Liu, Suzanne M Gilboa, et al.American Journal of Medical Genetics. Part A|November 28, 2014
Aortopathy in the 7q11.23 microduplication syndromeAshley Parrott, Jeanne James, Paula Goldenberg, et al.Statistics in Medicine|February 9, 2016
Bayesian multinomial probit modeling of daily windows of susceptibility for maternal PM2.5 exposure and congenital heart defectsJoshua L Warren, Jeanette A Stingone, Amy H Herring, et al.American Journal of Medical Genetics|July 13, 2002
Childhood-onset ataxia: testing for large CAG-repeats in SCA2 and SCA7Rong Mao, Arthur S Aylsworth, Nicholas Potter, et al.Pageof 6