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Paper Details

Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric Medicine.
NPJ Genom Med
243
2016
CNV, CNVs, congenital malformations, genetic disorders, indels, insertion-deletions, neurodevelopmental disorders, patients
Author NameAffiliation
Ryan K C YuenThe Hospital for Sick Children
Ryan K C YuenThe Hospital for Sick Children
Michael J SzegoThe Hospital for Sick Children
Michael J SzegoUniversity of Toronto
Michael J SzegoDepartment of Family and Community Medicine and Clinical Public Health Division, University of Toronto
Randi Zlotnik ShaulUniversity of Toronto
Randi Zlotnik ShaulThe Hospital for Sick Children
Michael BrudnoThe Hospital for Sick Children
Michael BrudnoThe Hospital for Sick Children
Michael BrudnoUniversity of Toronto
Marta GirdeaThe Hospital for Sick Children
Marta GirdeaThe Hospital for Sick Children
Brendan J FreyUniversity of Toronto
Brendan J FreyUniversity of Toronto
Brendan J FreyUniversity of Toronto
Lauren ChadDivision of Clinical and Metabolic Genetics, The Hospital for Sick Children
Raymond H KimDivision of Clinical and Metabolic Genetics, The Hospital for Sick Children
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
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
Christian R MarshallThe Hospital for Sick Children
Christian R MarshallThe Hospital for Sick Children
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