The 37th episode of the Progress Educational Trust podcast explores how to improve access to genetic and genomic testing – and related services – for people and families affected by rare disease, featuring contributions from Dr Sarah Wynn, Miranda Durkie, Professor Emma Baple, Dr Ellen Thomas and Adam Clatworthy.
(If you can't see the podcast episode embedded below, you can listen to or download it via Spreaker.)
Listen to "Rare Disease Genomic Testing: How Do We Make Access Equitable and Timely?" on Spreaker.
You can also find us on podcast apps and platforms including Apple, Google, iHeart, Spotify and others. Just search for 'Progress Educational Trust podcast', and subscribe via the platform of your choice. Alternatively, look out for future podcast episodes in BioNews.
We would like to thank Jon Nicoll (who created the opening and closing music for our podcast), and also the NIHR Exeter Biomedical Research Centre (which supported the event featured in the 37th episode).
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