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The impact of the 100,000 Genomes Project on rare disease in national healthcare

dc.contributor.authorSmedley, D
dc.contributor.authorAbbs, S
dc.contributor.authorArno, G
dc.contributor.authorBaple, E
dc.contributor.authorBarnes, M
dc.contributor.authorBeales, P
dc.contributor.authorBitner-Glindzicz, M
dc.contributor.authorBlack, G
dc.contributor.authorBrennan, P
dc.contributor.authorChan, G
dc.contributor.authorChinnery, P
dc.contributor.authorCipriani, V
dc.contributor.authorEllard, S
dc.contributor.authorEllingford, J
dc.contributor.authorElliott, P
dc.contributor.authorFirth, H
dc.contributor.authorFlintner, F
dc.contributor.authorGarikano, KI
dc.contributor.authorHoulden, H
dc.contributor.authorIrving, M
dc.contributor.authorJacobsen, J
dc.contributor.authorMcDonagh, E
dc.contributor.authorMcMullan, D
dc.contributor.authorMoutsianas, L
dc.contributor.authorNewman, W
dc.contributor.authorOuwehand, WH
dc.contributor.authorRatnaike, T
dc.contributor.authorMartin, AR
dc.contributor.authorPenkett, C
dc.contributor.authorRaymond, F
dc.contributor.authorSayer, J
dc.contributor.authorScott, R
dc.contributor.authorSmith, K
dc.contributor.authorStark, H
dc.contributor.authorStirrups, K
dc.contributor.authorTaylor, J
dc.contributor.authorThomas, E
dc.contributor.authorTucci, A
dc.contributor.authorVandrovcova, J
dc.contributor.authorVestito, L
dc.contributor.authorWebster, A
dc.contributor.authorWei, W
dc.contributor.authorWielscher, M
dc.contributor.authorWilliams, H
dc.contributor.authorWilkie, A
dc.contributor.authorWright, C
dc.contributor.authorRendon, A
dc.contributor.authorCaulfield, M
dc.contributor.authorBioResource, NIHR
dc.contributor.authorConsortium, GER
dc.date.accessioned2021-02-08T15:13:25Z
dc.date.available2021-02-08T15:13:25Z
dc.date.issued2020-12
dc.identifier.citationAbstracts from the 53rd European Society of Human Genetics (ESHG) Conference: Oral Presentations. Eur J Hum Genet 28, 1–140 (2020). https://doi.org/10.1038/s41431-020-00740-6en_US
dc.identifier.issn1018-4813
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/70170
dc.description.abstractAbstract C08.6 from the 53rd European Society of Human Genetics (ESHG) Conferenceen_US
dc.format.extent54 - 55
dc.relation.ispartofEuropean journal of human genetics
dc.titleThe impact of the 100,000 Genomes Project on rare disease in national healthcareen_US
dc.typeConference Proceedingen_US
dc.identifier.doi10.1038/s41431-020-00740-6
pubs.author-urlhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000598482600112&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.issueSUPPL 1en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume28en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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