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dc.contributor.authorCangül, Hakan
dc.contributor.authorÖzel, Mavi Deniz
dc.contributor.authorGenç, Nimetullah Mete
dc.contributor.authorKardelen Al, Aslı Derya
dc.contributor.authorDarendeliler, Feyza
dc.date.accessioned2021-01-12T12:44:27Z
dc.date.available2021-01-12T12:44:27Z
dc.date.issued2018en_US
dc.identifier.citationCangül, H., Özel, M. D., Genç, N. M., Kardelen Al, A. D. ve Darendeliler, F. (2018). Development of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidism. 50th European-Society-of-Human-Genetics (ESHG) Conference içinde (198-198. ss.). Copenhagen, Denmark, May 27-30, 2017.en_US
dc.identifier.issn1018-4813
dc.identifier.issn1476-5438
dc.identifier.urihttps://hdl.handle.net/20.500.12511/6229
dc.description.abstract...en_US
dc.description.sponsorshipEuropean Society of Human Geneticsen_US
dc.language.isoengen_US
dc.publisherNature Publishing Groupen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCongenital Hypothyroidismen_US
dc.subjectGenetic Testen_US
dc.subjectDiagnosisen_US
dc.titleDevelopment of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidismen_US
dc.typeconferenceObjecten_US
dc.relation.journal50th European-Society-of-Human-Genetics (ESHG) Conferenceen_US
dc.departmentİstanbul Medipol Üniversitesi, Uluslararası Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Tıbbi Genetik Ana Bilim Dalıen_US
dc.departmentİstanbul Medipol Üniversitesi, Uluslararası Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Tıbbi Biyoloji Ana Bilim Dalıen_US
dc.identifier.volume26en_US
dc.identifier.issueSupplement: Sen_US
dc.identifier.startpage198en_US
dc.identifier.endpage198en_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US


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