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Paper Details

Dominant-negative variants in CBX1 cause a neurodevelopmental disorder.
Genet Med
2
2023
Author NameAffiliation
Suzanna E L TemplePrince of Wales Hospital, Australia Centre for Clinical Genetics, Sydney Children's Hospital
Daniel C KoboldtThe Steve and Cindy Rasmussen Institute for Genomic Medicine, Nationwide Children's Hospital, The Ohio State University College of Medicine
Gopinath M SubramanianJohn Hunter Children's Hospital
Kandamurugu ManickamThe Ohio State University College of Medicine, Nationwide Children's Hospital
Elaine H ZackaiThe Children's Hospital of Philadelphia, Perelman School of Medicine at the University of Pennsylvania
Matthew C DulikThe Children's Hospital of Philadelphia, Perelman School of Medicine at the University of Pennsylvania
Tony RoscioliPrince of Wales Hospital, Australia Neuroscience Research Australia (NeuRA) and Prince of Wales Clinical School, University of New South Wales
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