Showing results (51-60 of 138) with videos related to
Sort By:
Pageof 14
American Journal of Human Genetics|November 27, 2015
Histone Modifier Genes Alter Conotruncal Heart Phenotypes in 22q11.2 Deletion SyndromeTingwei Guo, Jonathan H Chung, Tao Wang, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 17, 2018
Musical auditory processing, cognition, and psychopathology in 22q11.2 deletion syndromeLucy Gao, Sunny X Tang, James J Yi, et al.European Journal of Medical Genetics|March 18, 2008
Atypical 22q11.2 deletion in a patient with DGS/VCFS spectrumSintia Iole Nogueira, April M Hacker, Fernanda T S Bellucco, et al.The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 21, 2006
Evaluation of potential modifiers of the palatal phenotype in the 22q11.2 deletion syndromeDeborah A Driscoll, Torrey Boland, Beverly S Emanuel, et al.Birth Defects Research|June 22, 2019
Copy number variations in individuals with conotruncal heart defects reveal some shared developmental pathways irrespective of 22q11.2 deletion statusHongbo M Xie, Deanne M Taylor, Zhe Zhang, et al.Schizophrenia Bulletin|October 18, 2017
Attention Deficit Hyperactivity Disorder Symptoms and Psychosis in 22q11.2 Deletion SyndromeMaria Niarchou, Monica E Calkins, Tyler M Moore, et al.Journal of Psychiatric Research|April 24, 2017
The dimensional structure of psychopathology in 22q11.2 Deletion SyndromeMaria Niarchou, Tyler M Moore, Sunny X Tang, et al.Molecular Cytogenetics|December 6, 2014
Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocationDivya Mishra, Takema Kato, Hidehito Inagaki, 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.Proceedings of the National Academy of Sciences of the United States of America|June 7, 2007
Systematic prediction and validation of breakpoints associated with copy-number variants in the human genomeJan O Korbel, Alexander Eckehart Urban, Fabian Grubert, et al.Pageof 14