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

dc.contributor.authorOzel, M.
dc.contributor.authorKardelen, A. D.
dc.contributor.authorGenc, N.
dc.contributor.authorDarendeliler, F.
dc.contributor.authorCangul, H.
dc.date.accessioned2021-03-03T16:45:07Z
dc.date.available2021-03-03T16:45:07Z
dc.identifier.citationCangul H., Ozel M., Genc N., Kardelen A. D. , Darendeliler F., "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, Copenhagen, Danimarka, 27 - 30 Mayıs 2017, cilt.26, ss.198
dc.identifier.othervv_1032021
dc.identifier.otherav_45fa8112-62b8-4f22-b4fc-aaf0d7372d99
dc.identifier.urihttp://hdl.handle.net/20.500.12627/50672
dc.language.isoeng
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectSitogenetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTemel Bilimler
dc.subjectGENETİK VE HAYAT
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.titleDevelopment of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidism
dc.typeBildiri
dc.contributor.departmentİstanbul Medipol Üniversitesi , ,
dc.identifier.volume26
dc.contributor.firstauthorID154617


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