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Uniparental disomy in the Rare Disease Programme of the UK's 100,000 Genomes Project

dc.contributor.authorSmith, KRen_US
dc.contributor.authorBleda, Men_US
dc.contributor.authorKasperaviciute, Den_US
dc.contributor.authorIbanez, Ken_US
dc.contributor.authorMartin, ARen_US
dc.contributor.authorThomas, Een_US
dc.contributor.authorBaple, Een_US
dc.contributor.authorTucci, Aen_US
dc.contributor.authorCaulfield, MJen_US
dc.contributor.authorRendon, Aen_US
dc.date.accessioned2020-10-05T10:29:10Z
dc.date.available2019-08-01en_US
dc.date.issued2019-10en_US
dc.identifier.issn1018-4813en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/67378
dc.format.extent1153 - 1154en_US
dc.titleUniparental disomy in the Rare Disease Programme of the UK's 100,000 Genomes Projecten_US
dc.typeConference Proceeding
pubs.author-urlhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000489313900206&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume27en_US


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