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Annals of Human Genetics|July 5, 2025
The Promise and Challenges of Genomics for Patients and Families Affected by Rare ConditionsClaire A Andersen, Anna L Pelling, Sarah L Wynn
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|July 3, 2025
Identifying the Impacts, Obstacles and Information Barriers for Parents of Children Living With Genetic Neurodevelopmental Disorders: A Qualitative StudyKaren J Low, , Georgia Treneman-Evans, et al.
BMJ Open|May 17, 2024
Improving the care of children with GENetic Rare disease: Observational Cohort study (GenROC)-a study protocolKaren Jaqueline Low, Amy Watford, Peter Blair, et al.
Nature Neuroscience|September 28, 2010
SOX9 induces and maintains neural stem cellsCharlotte E Scott, Sarah L Wynn, Abdul Sesay, et al.
European Journal of Human Genetics : EJHG|October 3, 2024
Equity and timeliness as factors in the effectiveness of an ethical prenatal sequencing service: reflections from parents and professionalsMichelle Peter, Melissa Hill, Jane Fisher, et al.
NIHR Open Research|October 25, 2023
Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocolCeline Lewis, James Buchanan, Angus Clarke, et al.
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