dc.contributor.author | Cangül, Hakan | |
dc.contributor.author | Özel, Mavi Deniz | |
dc.contributor.author | Genç, Nimetullah Mete | |
dc.contributor.author | Kardelen Al, Aslı Derya | |
dc.contributor.author | Darendeliler, Feyza | |
dc.date.accessioned | 2021-01-12T12:44:27Z | |
dc.date.available | 2021-01-12T12:44:27Z | |
dc.date.issued | 2018 | en_US |
dc.identifier.citation | Cangül, 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.issn | 1018-4813 | |
dc.identifier.issn | 1476-5438 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12511/6229 | |
dc.description.abstract | ... | en_US |
dc.description.sponsorship | European Society of Human Genetics | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Nature Publishing Group | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Congenital Hypothyroidism | en_US |
dc.subject | Genetic Test | en_US |
dc.subject | Diagnosis | en_US |
dc.title | Development of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidism | en_US |
dc.type | conferenceObject | en_US |
dc.relation.ispartof | 50th European-Society-of-Human-Genetics (ESHG) Conference | en_US |
dc.department | İstanbul Medipol Üniversitesi, Uluslararası Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Tıbbi Genetik Ana Bilim Dalı | en_US |
dc.department | İstanbul Medipol Üniversitesi, Uluslararası Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Tıbbi Biyoloji Ana Bilim Dalı | en_US |
dc.identifier.volume | 26 | en_US |
dc.identifier.issue | Supplement: S | en_US |
dc.identifier.startpage | 198 | en_US |
dc.identifier.endpage | 198 | en_US |
dc.relation.publicationcategory | Konferans Öğesi - Uluslararası - Kurum Öğretim Elemanı | en_US |
dc.identifier.wosquality | Q2 | en_US |