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The G67E mutation in hMLH1 is associated with an unusual presentation of Lynch syndrome

dc.contributor.authorClyne, Men_US
dc.contributor.authorOffman, Jen_US
dc.contributor.authorShanley, Sen_US
dc.contributor.authorVirgo, JDen_US
dc.contributor.authorRadulovic, Men_US
dc.contributor.authorWang, Yen_US
dc.contributor.authorArdern-Jones, Aen_US
dc.contributor.authorEeles, Ren_US
dc.contributor.authorHoffmann, Een_US
dc.contributor.authorYu, VPCCen_US
dc.date.accessioned2017-06-16T14:22:01Z
dc.date.issued2009-01-22en_US
dc.date.submitted2017-05-04T08:38:07.723Z
dc.identifier.issn0007-0920en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/24370
dc.format.extent376 - 380en_US
dc.language.isoenen_US
dc.relation.ispartofBRITISH JOURNAL OF CANCERen_US
dc.rightsCC-BY-NC-SA
dc.subjectG67Een_US
dc.subjectHNPCCen_US
dc.subjecthMLH1en_US
dc.subjectbreasten_US
dc.subjectprostateen_US
dc.titleThe G67E mutation in hMLH1 is associated with an unusual presentation of Lynch syndromeen_US
dc.typeArticle
dc.rights.holder© 2009, Rights Managed by Nature Publishing Group
dc.identifier.doi10.1038/sj.bjc.6604860en_US
pubs.author-urlhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000262637800023&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.issue2en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume100en_US


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