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

Cangül, HakanÖzel, Mavi DenizGenç, Nimetullah MeteKardelen Al, Aslı DeryaDarendeliler, Feyza2021-01-122021-01-122018Cangül, 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, 2017.1018-48131476-5438https://hdl.handle.net/20.500.12511/6229[Abstract Not Available]eninfo:eu-repo/semantics/closedAccessCongenital HypothyroidismGenetic TestDiagnosisDevelopment of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidismConference Object26Supplement: S198198Q2