Novel PTCH1 Gene Mutation in a Patient with Gorlin-Goltz Syndrome

Özlü, EminKaradağ, Ayşe SerapAkalın, İbrahimYeşil, GözdeYılmaz, SarenurZindancı, İlkinAkdeniz, Necmettin2020-04-302020-04-3020191013-90872005-3894https://doi.org/10.5021/ad.2019.31.S.S10https://hdl.handle.net/20.500.12684/3839WOS: 000524236100005…en10.5021/ad.2019.31.S.S10info:eu-repo/semantics/closedAccessNovel PTCH1 Gene Mutation in a Patient with Gorlin-Goltz SyndromeEditorial31S10S11WOS:000524236100005Q3