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Whole Exome Sequencing can Identify Defects not Detected by Candidate Gene Sequencing in Patients with Short Stature and Features of Growth Hormone Insensitivity (GHI)

dc.contributor.authorShapiro, Len_US
dc.contributor.authorSavage, Men_US
dc.contributor.authorDavies, Ken_US
dc.contributor.authorMetherell, Len_US
dc.contributor.authorStorr, Hen_US
dc.date.accessioned2017-07-07T14:39:52Z
dc.date.issued2016en_US
dc.date.submitted2017-03-23T14:22:54.095Z
dc.identifier.issn1663-2818en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/24789
dc.format.extent47 - 47en_US
dc.language.isoenen_US
dc.rightsPublished version is available at https://www.karger.com/Article/Pdf/449141
dc.titleWhole Exome Sequencing can Identify Defects not Detected by Candidate Gene Sequencing in Patients with Short Stature and Features of Growth Hormone Insensitivity (GHI)en_US
dc.typeConference Proceeding
dc.rights.holder© 2016 S. Karger AG, Basel
pubs.author-urlhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000384166800113&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume86en_US


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