Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocol [version 2; peer review: 2 approved, 2 approved with reservations]

Celine Lewis,James Buchanan,Angus Clarke,Emma Clement,Bettina Friedrich,Jillian Hastings-Ward,Melissa Hill,Ruth Horn,Anneke M. Lucassen,Chris Patch,Alexandra Pickard,Lauren Roberts,Saskia C. Sanderson,Sarah L. Wynn,Cecilia Vindrola-Padros,Monica Lakhanpaul

semanticscholar（2022）

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摘要

Background: A new nationally commissioned NHS England Genomic Medicine Service (GMS) was recently established to deliver genomic testing with equity of access for patients affected by rare diseases and cancer. The overarching aim of this research is to evaluate the implementation of the GMS during its early years, identify barriers Open Peer Review

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