Optimising rapid prenatal exome sequencing in the NHS genomic medicine service: the EXPRESS Synopsis

Background Prenatal exome sequencing for the diagnosis of fetal anomalies was implemented nationally in England in October 2020 by the National Health Service Genomic Medicine Service. Objective To evaluate the new prenatal exome sequencing service to provide evidence that will inform improvements t...

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Detalhes bibliográficos

Principais autores:	Melissa Hill, Michelle Peter, Morgan Daniel, Hannah McInnes-Dean, Rema Ramakrishnan, Emma Smith, Holly Walton, Laura Blackburn, Jane Fisher, Naomi J Fulop, Marian Knight, Caroline Lafarge, Kerry Leeson-Beevers, Rhiannon Mellis, Stephen Morris, Michael Parker, Sophie Peet, Dagmar Tapon, Wing Han Wu, Sarah L Wynn, Lyn S Chitty
Formato:	Artigo
Idioma:	Inglês
Publicado em:	NIHR Journals Library 2026-04-01
coleção:	Health and Social Care Delivery Research
Assuntos:	prenatal exome sequencing mixed-methods ethics cost-effectiveness implementation major system change genomics
Acesso em linha:	https://doi.org/10.3310/GJLC0716
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