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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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Kaydedildi:
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: NIHR Journals Library 2026-04-01
Seri Bilgileri:Health and Social Care Delivery Research
Konular:
prenatal exome sequencing
mixed-methods
ethics
cost-effectiveness
implementation
major system change
genomics
Online Erişim:https://doi.org/10.3310/GJLC0716
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