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Rare CNVs provide novel insights into the molecular basis of GH and IGF-1 insensitivity

dc.contributor.authorCottrell, E
dc.contributor.authorCabrera, CP
dc.contributor.authorIshida, M
dc.contributor.authorChatterjee, S
dc.contributor.authorGreening, J
dc.contributor.authorWright, N
dc.contributor.authorBossowski, A
dc.contributor.authorDunkel, L
dc.contributor.authorDeeb, A
dc.contributor.authorAl Basiri, I
dc.contributor.authorRose, SJ
dc.contributor.authorMason, A
dc.contributor.authorBint, S
dc.contributor.authorAhn, JW
dc.contributor.authorHwa, V
dc.contributor.authorMetherell, LA
dc.contributor.authorMoore, GE
dc.contributor.authorStorr, HL
dc.date.accessioned2020-11-16T11:25:50Z
dc.date.available2020-09-17
dc.date.available2020-11-16T11:25:50Z
dc.date.issued2020-12
dc.identifier.citationCottrell, E., Cabrera, C., Ishida, M., Chatterjee, S., Greening, J., Wright, N., Bossowski, A., Dunkel, L., Deeb, A., Basiri, I., Rose, S., Mason, A., Bint, S., Ahn, J., Hwa, V., Metherell, L., Moore, G., & Storr, H. (2020). Rare CNVs provide novel insights into the molecular basis of GH and IGF-1 insensitivity, European Journal of Endocrinology, 183(6), 581-595. Retrieved Nov 16, 2020, from https://eje.bioscientifica.com/view/journals/eje/183/6/EJE-20-0474.xmlen_US
dc.identifier.issn0804-4643
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/68318
dc.description“Disclaimer: this is not the definitive version of record of this article. This manuscript has been accepted for publication in European Journal of Endocrinology, but the version presented here has not yet been copy-edited, formatted or proofed. The definitive version is will be freely available at https://doi.org/10.1530/EJE-20-0474, 2020.”en_US
dc.format.extent581 - 595
dc.language.isoenen_US
dc.relation.ispartofEUROPEAN JOURNAL OF ENDOCRINOLOGY
dc.titleRare CNVs provide novel insights into the molecular basis of GH and IGF-1 insensitivityen_US
dc.typeArticleen_US
dc.identifier.doi10.1530/EJE-20-0474
pubs.author-urlhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000579830800010&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.issue6en_US
pubs.notesNot knownen_US
pubs.publication-statusAccepteden_US
pubs.volume183en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US
qmul.funderImproved genetic diagnosis of primary adrenal insufficiency::Barts Charityen_US


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