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Paper Details

Variable phenotype expression in a family segregating microdeletions of the <i>NRXN1</i> and <i>MBD5</i> autism spectrum disorder susceptibility genes.
NPJ Genom Med
29
2017
ASD, Autism Spectrum Disorder, CNV, CNV microdeletions, CNVs, MBD5, NRXN1, SNVs, SVs, autism spectrum disorder, autism spectrum disorder susceptibility genes, developmental condition, exon overlapping variants, genomic loci, indels, neurodevelopmental disorders, single nucleotide variants
Author NameAffiliation
Marc Woodbury-SmithMcMaster University
Marc Woodbury-SmithThe Hospital for Sick Children
Mehdi ZarreiThe Hospital for Sick Children
Ryan K C YuenThe Hospital for Sick Children
Susan WalkerThe Hospital for Sick Children
Ann ThompsonMcMaster University
Peter SzatmariThe Hospital for Sick Children & University of Toronto
Peter SzatmariThe Hospital for Sick Children & University of Toronto
Stephen W SchererThe Hospital for Sick Children
Stephen W SchererUniversity of Toronto
Stephen W SchererThe Hospital for Sick Children
Stephen W SchererUniversity of Toronto
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