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Pediatrics in Review|September 4, 2009
The floppy infant: evaluation of hypotoniaDawn E Peredo, Mark C HannibalPlos One|May 27, 2010
Alternative splicing of sept9a and sept9b in zebrafish produces multiple mRNA transcripts expressed throughout developmentMegan L Landsverk, Douglas C Weiser, Mark C Hannibal, et al.Pediatric Cardiology|July 11, 2006
Aortic root dilatation is a rare complication of Noonan syndromePatricia D Power, Mark B Lewin, Mark C Hannibal, et al.Lymphatic Research and Biology|November 27, 2007
Clinical outcomes in lymphocytopenic lymphatic malformation patientsJonathan A Perkins, Richard M Tempero, Mark C Hannibal, et al.Pediatric Neurology|April 12, 2021
Symptom Prevalence and Genotype-Phenotype Correlations in Patients With TANGO2-Related Metabolic Encephalopathy and Arrhythmias (TRMEA)Allison R Powell, Elizabeth G Ames, Erin Neil Knierbein, et al.American Journal of Medical Genetics. Part A|April 2, 2022
Novel multilocus imprinting disturbances in a child with expressive language delay and intellectual disabilityMarwan K Tayeh, Janean DeVaul, Kristin LeSueur, et al.The American Journal of Surgical Pathology|September 28, 2010
Diffuse abnormal layering of small intestinal smooth muscle is present in patients with FLNA mutations and x-linked intestinal pseudo-obstructionRaj P Kapur, Stephen P Robertson, Mark C Hannibal, et al.Journal of Pediatric Hematology/Oncology|October 30, 2020
The Use of B-Cell Polysome Profiling to Validate Novel RPL5 (uL18) and RPL26 (uL24) Variants in Diamond-Blackfan AnemiaAlexander Ludlow, Nicholas George, Megan Glassford, et al.Molecular Cytogenetics|May 13, 2008
Unexpected structural complexity of supernumerary marker chromosomes characterized by microarray comparative genomic hybridizationKaren D Tsuchiya, Kent E Opheim, Mark C Hannibal, et al.Human Molecular Genetics|December 10, 2015
De novo dominant ASXL3 mutations alter H2A deubiquitination and transcription in Bainbridge-Ropers syndromeAnshika Srivastava, K C Ritesh, Yao-Chang Tsan, et al.Pageof 3