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Mutations in WNT1 cause different forms of bone fragility

dc.contributor.authorKornak, Uwe
dc.contributor.authorAmling, Michael
dc.contributor.authorMarini, Joan
dc.contributor.authorWollnik, Bernd
dc.contributor.authorKayserili, Hulya
dc.contributor.authorKeupp, Katharina
dc.contributor.authorBeleggia, Filippo
dc.contributor.authorBarnes, Aileen
dc.contributor.authorSteiner, Magdalena
dc.contributor.authorSemler, Oliver
dc.contributor.authorLausch, Ekkehart
dc.contributor.authorBreer, Stefan
dc.contributor.authorSchoenau, Eckhard
dc.contributor.authorSchinke, Thorsten
dc.contributor.authorZabel, Bernhard
dc.contributor.authorMundlos, Stefan
dc.date.accessioned2021-03-04T11:51:43Z
dc.date.available2021-03-04T11:51:43Z
dc.identifier.citationKeupp K., Beleggia F., Kayserili H., Barnes A., Steiner M., Semler O., Lausch E., Breer S., Schoenau E., Schinke T., et al., "Mutations in WNT1 cause different forms of bone fragility", Annual Meeting of the American-Society-for-Bone-and-Mineral-Research, Maryland, Amerika Birleşik Devletleri, 4 - 07 Ekim 2013, cilt.28
dc.identifier.othervv_1032021
dc.identifier.otherav_747bc7f3-4f7e-48ec-9b8a-f45f30f049c9
dc.identifier.urihttp://hdl.handle.net/20.500.12627/80060
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectEndokrinoloji ve Metabolizma Hastalıkları
dc.subjectENDOKRİNOLOJİ VE METABOLİZMA
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.titleMutations in WNT1 cause different forms of bone fragility
dc.typeBildiri
dc.contributor.departmentUniversity of Cologne , ,
dc.identifier.volume28
dc.contributor.firstauthorID141255


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