Development of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidism

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.issued2018
dc.departmentİstanbul Medipol Üniversitesi, Uluslararası Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Tıbbi Genetik Ana Bilim Dalı
dc.departmentİstanbul Medipol Üniversitesi, Uluslararası Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Tıbbi Biyoloji Ana Bilim Dalı
dc.description.abstract[Abstract Not Available]
dc.description.sponsorshipEuropean Society of Human Geneticsen_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.
dc.identifier.endpage198
dc.identifier.issn1018-4813
dc.identifier.issn1476-5438
dc.identifier.issueSupplement: S
dc.identifier.startpage198
dc.identifier.urihttps://hdl.handle.net/20.500.12511/6229
dc.identifier.volume26
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.language.isoen
dc.publisherNature Publishing Group
dc.relation.ispartof50th European-Society-of-Human-Genetics (ESHG) Conferenceen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectCongenital Hypothyroidism
dc.subjectGenetic Test
dc.subjectDiagnosis
dc.titleDevelopment of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidism
dc.typeConference Object

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