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Paper Details

SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing.
Hum Genet
2
2023
CNV, CNVs, Copy number variants, SCIP, autism spectrum disorder, congenital cardiac disease, copy number variants, pathogenic CNV, rare genetic diseases
Author NameAffiliation
Mehdi ZarreiThe Hospital for Sick Children
Mehdi ZarreiThe Hospital for Sick Children
Stephen W SchererThe Hospital for Sick Children
Stephen W SchererUniversity of Toronto
Stephen W SchererThe Hospital for Sick Children
Stephen W SchererThe Hospital for Sick Children
Stephen W SchererThe Hospital for Sick Children
Stephen W SchererUniversity of Toronto
Raymond H KimCardiac Genome Clinic, The Hospital for Sick Children
Raymond H KimDivision of Clinical and Metabolic Genetics, The Hospital for Sick Children
Raymond H KimUniversity Health Network
Raymond H KimUniversity of Toronto
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