Both deletion and duplication of human chromosome 7q11.23 cause neurodevelopmental disorders with unique phenotypic profiles, so offering a window into the genetics of human behaviour, cognition and language. We use mouse models and the genetic analysis of human subjects to probe the underlying molecular basis of these disorders.
- MMG1222: Human Genome Analysis
- Tier 1 Canada Research Chair in the Genetics of Neurodevelopmental Disorders
- Department of Medicine
- Institute of Medical Science
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