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The Journal of Thoracic and Cardiovascular Surgery|February 14, 2014
Neurodevelopmental outcomes in preschool survivors of the Fontan procedureJ William Gaynor, Richard F Ittenbach, Marsha Gerdes, et al.American Journal of Medical Genetics|June 26, 2001
Bilateral microtia and cleft palate in cousins with Diamond-Blackfan anemiaK W Gripp, D M McDonald-McGinn, D La Rossa, et al.American Journal of Medical Genetics. Part A|August 14, 2014
Congenital microcephaly and chorioretinopathy due to de novo heterozygous KIF11 mutations: five novel mutations and review of the literatureGhayda M Mirzaa, Laura Enyedi, Gretchen Parsons, et al.Pediatrics|March 4, 2008
Neurodevelopmental outcomes after staged palliation for hypoplastic left heart syndromeSarah Tabbutt, Alex S Nord, Gail P Jarvik, et al.Pediatrics|May 11, 1997
Detection of a 22q11.2 deletion in cardiac patients suggests a risk for velopharyngeal incompetenceD M McDonald-McGinn, D A Driscoll, B S Emanuel, et al.American Journal of Human Genetics|March 3, 2015
Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic featuresEmma Tham, Anna Lindstrand, Avni Santani, et al.AJNR. American Journal of Neuroradiology|September 3, 1998
Imaging studies in a unique familial dysmyelinating disorderK W Gripp, R A Zimmerman, Z J Wang, et al.Human Molecular Genetics|May 15, 2015
Kabuki syndrome genes KMT2D and KDM6A: functional analyses demonstrate critical roles in craniofacial, heart and brain developmentPeter M Van Laarhoven, Leif R Neitzel, Anita M Quintana, et al.Development and Psychopathology|November 3, 2005
A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in childrenTony J Simon, Joel P Bish, Carrie E Bearden, et al.Translational Psychiatry|July 26, 2017
Emergent, remitted and persistent psychosis-spectrum symptoms in 22q11.2 deletion syndromeS X Tang, T M Moore, M E Calkins, et al.Pageof 63