Successful integration of newborn genetic testing into UK routine screening using prospective consent to determine eligibility for clinical trials.

Archives of disease in childhood(2023)

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摘要
The use of prospective consent to perform personalised genetic testing on samples obtained through the routine NBSP represents a novel mechanism for clinical genetic research in the UK and provides a model for further population-based genetic studies in the newborn.
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endocrinology,genetics,neonatology,paediatrics
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