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dc.contributor.authorA, Aen_US
dc.contributor.authorA, Men_US
dc.contributor.authorE, Cen_US
dc.contributor.authorS, Cen_US
dc.contributor.authorP, Sen_US
dc.contributor.authorL, Den_US
dc.contributor.authorK, Den_US
dc.contributor.authorA, Ben_US
dc.contributor.authorT, Men_US
dc.contributor.authorR, Ven_US
dc.contributor.authorM, Den_US
dc.contributor.authorN, Sen_US
dc.contributor.authorLA, Men_US
dc.contributor.authorMO, Sen_US
dc.contributor.authorHL, Sen_US
dc.date.accessioned2023-03-21T10:58:37Z
dc.identifier.issn1662-4009en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/85103
dc.publisherBioscientificaen_US
dc.titleGenetic characterization of short stature patients with overlapping features of growth hormone insensitivity syndromesen_US
dc.typeArticle
dc.identifier.doi10.1530/ey.19.4.10en_US
pubs.notesNot knownen_US
qmul.funderImproved genetic diagnosis of primary adrenal insufficiency::Barts Charityen_US


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