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Human Genetics|July 14, 2006
Complex patterns of copy number variation at sites of segmental duplications: an important category of structural variation in the human genomeViolaine Goidts, David N Cooper, Lluis Armengol, et al.Plos Computational Biology|August 27, 2016
The Loss and Gain of Functional Amino Acid Residues Is a Common Mechanism Causing Human Inherited DiseaseJose Lugo-Martinez, Vikas Pejaver, Kymberleigh A Pagel, et al.Clinical Genetics|February 13, 2001
Resolution of a mispaired secondary structure intermediate could account for a novel micro-insertion/deletion (387 insA/del 8 bp) in the PYGM gene causing McArdle's diseaseM A Martín, J C Rubio, A García, et al.BMC Pediatrics|February 24, 2018
Health care quality measures for children and adolescents in Foster Care: feasibility testing in electronic recordsKatherine J Deans, Peter C Minneci, Kristine M Nacion, et al.Journal of Neurophysiology|July 25, 2008
Recovery from monocular deprivation using binocular deprivationBrian S Blais, Mikhail Y Frenkel, Scott R Kuindersma, et al.Genome Research|January 1, 2009
Splicing factor SFRS1 recognizes a functionally diverse landscape of RNA transcriptsJeremy R Sanford, Xin Wang, Matthew Mort, et al.Molecular Psychiatry|May 30, 2012
A new paradigm emerges from the study of de novo mutations in the context of neurodevelopmental diseaseC S Ku, C Polychronakos, E K Tan, et al.The Journal of Surgical Research|May 28, 2015
Utilization and costs associated with robotic surgery in childrenJustin B Mahida, Jennifer N Cooper, Daniel Herz, et al.Journal of Clinical Medicine|April 13, 2024
Landscape of NRXN1 Gene Variants in Phenotypic Manifestations of Autism Spectrum Disorder: A Systematic ReviewJaimee N Cooper, Jeenu Mittal, Akhila Sangadi, et al.BMC Pulmonary Medicine|March 18, 2022
Implementation of a strategy to facilitate effective medical follow-up for Australian First Nations children hospitalised with lower respiratory tract infections: study protocolAndré Schultz, Anne B Chang, Fenella Gill, et al.Pageof 125