Implementing genomic newborn screening as an effective public health intervention: sidestepping the...
Implementing genomic newborn screening as an effective public health intervention: sidestepping the hype and criticism
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Publisher
London: Nature Publishing Group UK
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Language
English
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London: Nature Publishing Group UK
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Contents
Genome-wide sequencing of the DNA that can be obtained from a newborn screening blood spot could provide predictions of thousands of genetic diseases that are not currently included in universal newborn screening. Most of the serious ethical, legal, privacy, and social concerns raised by genome sequencing of all infants can be avoided by implementi...
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Full title
Implementing genomic newborn screening as an effective public health intervention: sidestepping the hype and criticism
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TN_cdi_doaj_primary_oai_doaj_org_article_096e70e163c543fa85103c2693369235
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_096e70e163c543fa85103c2693369235
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ISSN
2056-7944
E-ISSN
2056-7944
DOI
10.1038/s41525-024-00451-7
