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Paper Details

Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care.
Clin Genet
272
2016
FORGE, childhood-onset disorders, children, disease genes, genetic diseases, novel gene, odyssey, patient, patients, rare genetic disease
Author NameAffiliation
Taila HartleyChildren's Hospital of Eastern Ontario Research Institute, University of Ottawa
Chandree L BeaulieuChildren's Hospital of Eastern Ontario Research Institute, University of Ottawa
Bridget A FernandezMemorial University of Newfoundland
Bridget A FernandezMemorial University of Newfoundland
Nada JabadoMcGill University
Nada JabadoMcGill University
Raymond H KimDivision of Clinical and Metabolic Genetics, The Hospital for Sick Children and University of Toronto
Raymond H KimUniversity of Toronto
Julie RicherChildren's Hospital of Eastern Ontario Research Institute, University of Ottawa
Guy A RouleauMontreal Neurological Institute, McGill University
Guy A RouleauMontreal Neurological Institute, McGill University
Mark A TarnopolskyMcMaster University
Kym M BoycottChildren's Hospital of Eastern Ontario Research Institute, University of Ottawa
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