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Toward the diagnosis of rare childhood genetic diseases: what do parents value most? (Apr, 10.1038/s41431-021-00925-7, 2021)

dc.contributor.authorPollard, Sen_US
dc.contributor.authorWeymann, Den_US
dc.contributor.authorDunne, Jen_US
dc.contributor.authorMayanloo, Fen_US
dc.contributor.authorBuckell, Jen_US
dc.contributor.authorBuchanan, Jen_US
dc.contributor.authorWordsworth, Sen_US
dc.contributor.authorFriedman, JMen_US
dc.contributor.authorStockler-Ipsiroglu, Sen_US
dc.contributor.authorDragojlovic, Nen_US
dc.contributor.authorElliott, AMen_US
dc.contributor.authorHarrison, Men_US
dc.contributor.authorLynd, LDen_US
dc.contributor.authorRegier, DAen_US
dc.date.accessioned2023-12-11T14:21:03Z
dc.date.issued2021en_US
dc.identifier.issn1018-4813en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/92802
dc.format.extent1589 - 1589en_US
dc.relation.ispartofEUROPEAN JOURNAL OF HUMAN GENETICSen_US
dc.titleToward the diagnosis of rare childhood genetic diseases: what do parents value most? (Apr, 10.1038/s41431-021-00925-7, 2021)en_US
dc.typeArticle
dc.identifier.doi10.1038/s41431-021-00925-7en_US
pubs.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000663258100001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.issue10en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume29en_US


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