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Paper Details

PhenomeCentral: 7 years of rare disease matchmaking.
Hum Mutat
11
2022
RD, RDs, candidate gene, genomic sequence, patient, patients, rare diseases
Author NameAffiliation
Taila HartleyChildren's Hospital of Eastern Ontario Research Institute, University of Ottawa
Marta GirdeaDATA Team and Techna Institute, University Health Network
Orion J Buske
Orion J Buske
Sergiu DumitriuDATA Team and Techna Institute, University Health Network
Kym M BoycottChildren's Hospital of Eastern Ontario Research Institute, University of Ottawa
Kym M BoycottChildren's Hospital of Eastern Ontario
Michael BrudnoDATA Team and Techna Institute, University Health Network
Michael BrudnoUniversity of Toronto
Michael BrudnoHospital for Sick Children
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