E. Ceylan

Vitamin D receptor gene polymorphisms in ocular surface squamous cell neoplasms

Nergiz A. Ismayilova, T. Akalın, T. Atik, 2020, European journal of ophthalmology.

What does white blood cells tell us at the first clinic visit of the cat

P. Ambarcioglu, O. S. Terzi, E. Ceylan, 2017 .

A rare cause of hydrops fetalis in two Gaucher disease type 2 patients with a novel mutation

A. Tukun, M. Başaranoğlu, S. Ceylaner, 2022, Metabolic brain disease.

A rare cause of hydrops fetalis in two Gaucher disease type 2 patients with a novel mutation

A. Tukun, M. Başaranoğlu, S. Ceylaner, 2022, Metabolic Brain Disease.

A novel Mecom gene mutation associated with amegakaryocytic thrombocytopenia in a premature infant.

N. Duman, H. Ören, A. Durmaz, 2022, The Turkish journal of pediatrics.