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Rare Disease Genomic Testing: How Do We Make Access Equitable and Timely?
This episode of the Progress Educational Trust (PET) podcast discusses how we might improve access to genetic and genomic testing, and related services, for people and families affected by rare disease.
The discussion is chaired by Sarah Norcross (Director of PET), with contributions from:
⚫ Dr Sarah Wynn (Chief Executive of Unique)
⚫ Miranda Durkie (Head of Rare Disease at the North East and Yorkshire Genomic Laboratory Hub)
⚫ Professor Emma Baple (Professor of Genomic Medicine at the University of Exeter)
⚫ Dr Ellen Thomas (Chief Medical Officer at Genomics England)
⚫ Adam Clatworthy…
The skinny
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