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Paper Details

Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees.
Am J Med Genet B Neuropsychiatr Genet
7
2020
ASD, Autism spectrum disorder, CNVs, DLGAP2, autism, autism spectrum disorder, copy number variations, neurodevelopmental disorder, rare CNV, synaptic scaffolding protein
Author NameAffiliation
Marc Woodbury-SmithTranslational and Clinical Research Institute, Newcastle University
Marc Woodbury-SmithThe Hospital for Sick Children
Mehdi ZarreiThe Hospital for Sick Children
Andrew D PatersonThe Hospital for Sick Children
Andrew D PatersonDalla Lana School of Public Health, University of Toronto
Ryan K C YuenThe Hospital for Sick Children
Ann ThompsonMcMaster University
Morgan ParlierCarolina Institute for Developmental Disabilities, University of North Carolina at Chapel Hill
Bridget A Fernandez
Bridget A Fernandez
Joseph PivenCarolina Institute for Developmental Disabilities, University of North Carolina at Chapel Hill
Stephen W SchererThe Hospital for Sick Children
Stephen W SchererUniversity of Toronto
Stephen W SchererThe Hospital for Sick Children
Stephen W SchererUniversity of Toronto
Veronica J VielandBattelle Center for Mathematical Medicine, The Research Institute at Nationwide Children's Hospital
Peter SzatmariThe Hospital for Sick Children & University of Toronto
Peter SzatmariThe Hospital for Sick Children & University of Toronto
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Release 1.2