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dc.contributor.authorBaşaran, Seher
dc.contributor.authorGökçay, Gülden Fatma
dc.contributor.authorKaraman, Birsen
dc.contributor.authorUyguner, Zehra Oya
dc.contributor.authorToksoy, Güven
dc.contributor.authorGedikbaşı, Asuman
dc.contributor.authorKaraca, Meryem
dc.contributor.authorBalcı, Mehmet Cihan
dc.contributor.authorGüleç, Çağrı
dc.contributor.authorSelamioğlu, Arzu
dc.date.accessioned2022-02-18T09:13:27Z
dc.date.available2022-02-18T09:13:27Z
dc.identifier.citationGedikbaşı A., Toksoy G., Karaca M., Balcı M. C. , Güleç Ç., Selamioğlu A., Karaman B., Başaran S., Gökçay G. F. , Uyguner Z. O. , "Diagnostic Utility of Whole Exome Sequencing in patients with suspected mitochondrial disease: the single center experience in Turkish population", International Congress on Inborn Errors in Metabolism (ICIEM), Sydney, Avustralya, 19 - 24 Kasım 2021, ss.1-3
dc.identifier.othervv_1032021
dc.identifier.otherav_25ef7411-becb-491d-9be2-1c90f44c901f
dc.identifier.urihttp://hdl.handle.net/20.500.12627/176774
dc.identifier.urihttps://avesis.istanbul.edu.tr/api/publication/25ef7411-becb-491d-9be2-1c90f44c901f/file
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp (MED)
dc.titleDiagnostic Utility of Whole Exome Sequencing in patients with suspected mitochondrial disease: the single center experience in Turkish population
dc.typeBildiri
dc.contributor.departmentİstanbul Üniversitesi , Çocuk Sağlığı Enstitüsü , Dahili Tıp Bilimleri Bölümü
dc.contributor.firstauthorID3039236


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