| dc.contributor.author | Da Costa, AR | |
| dc.contributor.author | Qarin, S | |
| dc.contributor.author | Bradshaw, TY | |
| dc.contributor.author | Watson, D | |
| dc.contributor.author | Prasad, R | |
| dc.contributor.author | Barnes, MR | |
| dc.contributor.author | Metherell, LA | |
| dc.contributor.author | Chapple, JP | |
| dc.contributor.author | Skarnes, WC | |
| dc.contributor.author | Storr, HL | |
| dc.date.accessioned | 2020-06-16T10:19:46Z | |
| dc.date.available | 2018-06-14 | |
| dc.date.available | 2020-06-16T10:19:46Z | |
| dc.date.issued | 2018 | |
| dc.identifier.issn | 1663-2818 | |
| dc.identifier.other | FC1.6 | |
| dc.identifier.uri | https://qmro.qmul.ac.uk/xmlui/handle/123456789/64999 | |
| dc.description.abstract | Meeting abstract FC1.6
from
57th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE) | en_US |
| dc.format.extent | 29 - 29 | |
| dc.publisher | Karger | en_US |
| dc.relation.ispartof | Hormone Research in Paediatrics | |
| dc.title | A Novel Stem Cell Model for the Triple a Syndrome | en_US |
| dc.type | Conference Proceeding | en_US |
| dc.identifier.doi | https://doi.org/10.1159/000492307 | |
| pubs.author-url | http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000445204100065&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6a | en_US |
| pubs.notes | Not known | en_US |
| pubs.publication-status | Published | en_US |
| pubs.volume | 90 | en_US |
| rioxxterms.funder | Default funder | en_US |
| rioxxterms.identifier.project | Default project | en_US |
| qmul.funder | Improved genetic diagnosis of primary adrenal insufficiency::Barts Charity | en_US |
