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STAG3 truncating variant as the cause of primary ovarian insufficiency

dc.contributor.authorStabej, PLQen_US
dc.contributor.authorWilliams, HJen_US
dc.contributor.authorJames, Cen_US
dc.contributor.authorTekman, Men_US
dc.contributor.authorStanescu, HCen_US
dc.contributor.authorKleta, Ren_US
dc.contributor.authorOcaka, Len_US
dc.contributor.authorLescai, Fen_US
dc.contributor.authorStorr, HLen_US
dc.contributor.authorBitner-Glindzicz, Men_US
dc.contributor.authorBacchelli, Cen_US
dc.contributor.authorConway, GSen_US
dc.contributor.authorGOSgeneen_US
dc.date.accessioned2017-03-31T12:54:47Z
dc.date.available2015-04-03en_US
dc.date.issued2016-01en_US
dc.date.submitted2017-03-23T12:39:17.294Z
dc.identifier.issn1018-4813en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/22342
dc.format.extent135 - 138en_US
dc.language.isoenen_US
dc.relation.ispartofEUROPEAN JOURNAL OF HUMAN GENETICSen_US
dc.rightsCC-BY
dc.titleSTAG3 truncating variant as the cause of primary ovarian insufficiencyen_US
dc.typeArticle
dc.rights.holder(c) 2016 Macmillan Publishers Limited
dc.identifier.doi10.1038/ejhg.2015.107en_US
pubs.author-urlhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000366615000021&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.issue1en_US
pubs.notesNo embargoen_US
pubs.notesOpen accessen_US
pubs.publication-statusPublisheden_US
pubs.volume24en_US


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