Gokhan Ozan Cetin

5PUBLICATIONS
21CO-AUTHORS
NeonatologyDevelopmental genetics (incl. sex determination)Vision scienceNeurology and neuromuscular diseasesGene mapping
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Publications (5)

|Apr 13, 2023
The clinical phenotype of Koolen-de Vries syndrome in Turkish patients and literature review.

Gokcen Karamik, Beyhan Tuysuz, Esra Isik

|Mar 31, 2023
Diagnostic and Management Strategies of Bietti Crystalline Dystrophy: Current Perspectives.

Ali Osman Saatci, Ferdane Ataş, Gökhan Ozan Çetin

|Jun 27, 2022
Early onset disease, anarthria, areflexia, and dystonia can be the distinctive features of SPG64, a very rare form of hereditary spastic paraplegias.

Akgün Ölmez, Gökhan Ozan Çetin, Kadri Karaer

|Dec 06, 2021
Genotype and phenotype characteristics of X-linked retinoschisis: the first report of a Turkish population.

Gokhan Ozan Cetin, Ebru Nevin Cetin, Tunahan Akyol

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