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Gorlin-Goltz Syndrome with a de novo variant in PTCH1: A case report

dc.contributor.authorAltunoğlu, Umut
dc.contributor.authorAksakal, Sermin Dicle
dc.contributor.authorİşler, Sabri Cemil
dc.contributor.authorKayserili Karabey, Hülya
dc.contributor.authorİmren, Ebru
dc.contributor.authorGüven, Yeliz
dc.date.accessioned2021-12-10T10:19:39Z
dc.date.available2021-12-10T10:19:39Z
dc.identifier.citationGüven Y., İmren E., Aksakal S. D. , İşler S. C. , Altunoğlu U., Kayserili Karabey H., "Gorlin-Goltz Syndrome with a de novo variant in PTCH1: A case report", The 28th Congress of the International Association of Paediatric Dentistry, 10 - 13 Haziran 2021, ss.1
dc.identifier.othervv_1032021
dc.identifier.otherav_38e03100-ed59-4658-8855-4a7fdc8defeb
dc.identifier.urihttp://hdl.handle.net/20.500.12627/169675
dc.language.isoeng
dc.subjectKlinik Tıp (MED)
dc.subjectSağlık Bilimleri
dc.titleGorlin-Goltz Syndrome with a de novo variant in PTCH1: A case report
dc.typeBildiri
dc.contributor.departmentİstanbul Üniversitesi , Diş Hekimliği Fakültesi , Klinik Bilimler Bölümü
dc.contributor.firstauthorID2724470


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