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Exploring the feasibility, acceptability and impact of genomic newborn screening for rare diseases in England: A study protocol for the Generation Study - Process and Impact Evaluation (Version 2)

2024-05-14

Abstract excerpt

The role of genomics in healthcare is expanding rapidly and many countries are exploring the possibility of using genomic sequencing to expand current newborn screening programmes. Offering routine genomic newborn screening (gNBS) would allow newborn screening to include a much broader range of rare conditions, but there are many technical, practical, psychosocial, ethical and economic challenges to be addressed....

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Literature Corpus work: dcc3017d-c49a-5a55-ad3d-58d237e5a472
DOI: 10.1101/2024.05.14.24307295

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