Gökhan Ozan Çetin (Gokhan Ozan Cetin)

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 5

Top Topics

Top Venues

American journal of medical genetics. Part A

Clinical ophthalmology (Auckland, N.Z.)

Ophthalmic genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Ali Osman Saatci, Ferdane Ataş, Gökhan Ozan Çetin, Mustafa Kayabaşı
Diagnostic and Management Strategies of Bietti Crystalline Dystrophy: Current Perspectives. Clinical ophthalmology (Auckland, N.Z.) 17 (2023)
Ali Osman Saatci, Ferdane Ataş, Gökhan Ozan Çetin, Mustafa Kayabaşı
Diagnostic and Management Strategies of Bietti Crystalline Dystrophy: Current Perspectives. Clinical ophthalmology (Auckland, N.Z.) 17 (2023)
Gokcen Karamik, Beyhan Tüysüz, Esra Isik, Aysegul Yilmaz, Yasemin Alanay, Evrim Cifci Sunamak, Enise Avci Durmusalioglu, Ferda Özkınay, Gökhan Ozan Çetin, Nuray Ozturk, Ercan Mihci, Banu Nur
The clinical phenotype of Koolen-de Vries syndrome in Turkish patients and literature review. American journal of medical genetics. Part A (2023)
Akgün Ölmez, Gökhan Ozan Çetin, Kadri Karaer
Early onset disease, anarthria, areflexia, and dystonia can be the distinctive features of SPG64, a very rare form of hereditary spastic paraplegias. American journal of medical genetics. Part A 188 (9) (2022)
Gökhan Ozan Çetin, Ebru Nevin Cetin, Tunahan Akyol, Hatice Deniz Ilhan, Gokhan Pekel
Genotype and phenotype characteristics of X-linked retinoschisis: the first report of a Turkish population. Ophthalmic genetics (2021)