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European guidance for the molecular diagnosis of pseudohypoparathyroidism not caused by point genetic variants at GNAS: an EQA study

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dc.contributor.authorDEMİRCİOĞLU, SERAP
dc.contributor.authorson behalf of the EuroPHP Consortium; Garin, Intza; Mantovani, Giovanna; Aguirre, Urko; Barlier, Anne; Brix, Bettina; Elli, Francesca M; Freson, Kathleen; Grybek, Virginie; Izzi, Benedetta; Linglart, Agnès; Perez de Nanclares, Guiomar; Silve, Caroline; Thiele, Susanne; Werner, Ralf
dc.date.accessioned2022-03-02T05:38:31Z
dc.date.accessioned2026-01-11T16:19:44Z
dc.date.available2022-03-02T05:38:31Z
dc.date.issued2015-04
dc.identifier.doi10.1038/ejhg.2014.127
dc.identifier.issn1018-4813, 1476-5438
dc.identifier.issue4
dc.identifier.pages438-444
dc.identifier.urihttps://hdl.handle.net/11424/218479
dc.identifier.volume23
dc.language.isoeng
dc.relation.urihttp://www.nature.com/articles/ejhg2014127
dc.titleEuropean guidance for the molecular diagnosis of pseudohypoparathyroidism not caused by point genetic variants at GNAS: an EQA study
dc.title.alternativeEuropean guidance for the molecular diagnosis of pseudohypoparathyroidism not caused by point genetic variants at GNAS
dc.typearticle
dspace.entity.typePublication

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