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Exploring the benefits, harms, and costs of genomic newborn screening for rare diseases

dc.contributor.authorBaple, EL
dc.contributor.authorScott, RH
dc.contributor.authorBanka, S
dc.contributor.authorBuchanan, J
dc.contributor.authorFish, L
dc.contributor.authorWynn, S
dc.contributor.authorWilkinson, D
dc.contributor.authorEllard, S
dc.contributor.authorMacArthur, DG
dc.contributor.authorStark, Z
dc.date.accessioned2024-05-10T10:29:31Z
dc.date.available2024-05-09
dc.date.available2024-05-10T10:29:31Z
dc.date.issued19-06-2024
dc.identifier.citationBaple, E.L., Scott, R.H., Banka, S. et al. Exploring the benefits, harms and costs of genomic newborn screening for rare diseases. Nat Med (2024). https://doi.org/10.1038/s41591-024-03055-x
dc.identifier.issn1546-170X
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/96780
dc.publisherNature Researchen_US
dc.relation.ispartofNature Medicine
dc.rightsThe version of record of this article, first published in Nature Medicine, is available online at Publisher’s website: doi.org/10.1038/s41591-024-03055-x
dc.titleExploring the benefits, harms, and costs of genomic newborn screening for rare diseasesen_US
dc.typeArticleen_US
dc.rights.holder© 2024, Springer Nature America, Inc.
dc.identifier.doidoi.org/10.1038/s41591-024-03055-x
pubs.notesNot knownen_US
pubs.publication-statusAccepteden_US
dcterms.dateAccepted2024-05-09
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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