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Ursie Smith

Medical Scientist

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Ursie has a long-term interest in rare disease and identified the gene for the rare neural tube defect Meckel-Gruber Syndrome (MKS) whilst doing her PhD in Child and Paediatric Health (University of Birmingham, 2006). Ursie also has significant front-line experience, working as an NHS doctor, with several years working in Oncology. Ursie is passionate about improving health outcomes in underrepresented populations.
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