dc.contributor.author |
Akin, Leyla |
|
dc.contributor.author |
Rizzoti, Karine |
|
dc.contributor.author |
Gregory, Louise C |
|
dc.contributor.author |
Corredor, Beatriz |
|
dc.contributor.author |
Le Quesne Stabej, Polona |
|
dc.contributor.author |
Williams, Hywel |
|
dc.contributor.author |
Buonocore, Federica |
|
dc.contributor.author |
Mouilleron, Stephane |
|
dc.contributor.author |
Capra, Valeria |
|
dc.contributor.author |
McGlacken-Byrne, Sinead M |
|
dc.contributor.author |
Martos-Moreno, Gabriel Á |
|
dc.contributor.author |
Azmanov, Dimitar N |
|
dc.contributor.author |
Kendirci, Mustafa |
|
dc.contributor.author |
Kurtoglu, Selim |
|
dc.contributor.author |
Suntharalingham, Jenifer P |
|
dc.contributor.author |
Galichet, Christophe |
|
dc.contributor.author |
Gustincich, Stefano |
|
dc.contributor.author |
Tasic, Velibor |
|
dc.contributor.author |
Achermann, John C |
|
dc.contributor.author |
Accogli, Andrea |
|
dc.contributor.author |
Filipovska, Aleksandra |
|
dc.contributor.author |
Tuilpakov, Anatoly |
|
dc.contributor.author |
Maghnie, Mohamad |
|
dc.contributor.author |
Gucev, Zoran |
|
dc.contributor.author |
Gonen, Zeynep Burcin |
|
dc.contributor.author |
Pérez-Jurado, Luis A |
|
dc.contributor.author |
Robinson, Iain |
|
dc.contributor.author |
Badge, Robin Lovell |
|
dc.contributor.author |
Argente, Jesús |
|
dc.contributor.author |
Dattani, Mehul T |
|
dc.date.accessioned |
2022-01-24T00:10:16Z |
|
dc.date.available |
2022-01-24T00:10:16Z |
|
dc.date.issued |
2021-11 |
|
dc.identifier.issn |
1098-3600 |
|
dc.identifier.uri |
https://hdl.handle.net/2292/58043 |
|
dc.language |
en |
|
dc.publisher |
Elsevier BV |
|
dc.relation.ispartofseries |
Genetics in Medicine |
|
dc.rights |
Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. |
|
dc.rights.uri |
https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm |
|
dc.subject |
0604 Genetics |
|
dc.subject |
1103 Clinical Sciences |
|
dc.title |
Pathogenic variants in RNPC3 are associated with hypopituitarism and primary ovarian insufficiency |
|
dc.type |
Journal Article |
|
dc.identifier.doi |
10.1016/j.gim.2021.09.019 |
|
dc.date.updated |
2021-12-01T09:45:42Z |
|
dc.rights.holder |
Copyright: The author |
en |
pubs.publication-status |
Published |
|
dc.rights.accessrights |
http://purl.org/eprint/accessRights/RestrictedAccess |
en |
pubs.subtype |
article |
|
pubs.elements-id |
875189 |
|