The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas

per Kurtulgan, Hande Küçük, Altuntaş, Emine Elif, Yıldırım, Malik Ejder, Özdemir, Öztürk, Bağcı, Binnur, Sezgin, İlhan
Publicat a J Int Adv Otol (2019)

Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia

per Yildirim, Malik Ejder, Kurtulgan, Hande Kucuk, Ozdemir, Ozturk, Kilicgun, Hasan, Aydemir, Didem S., Baser, Burak, Sezgin, Ilhan
Publicat a Ann Saudi Med (2019)

Recombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion

per Kurtulgan, Hande Küçük, Özer, Leyla, Yıldırım, Malik Ejder, Ünsal, Evrim, Aktuna, Süleyman, Baltacı, Volkan, Akkuş, Nejmiye, Sezgin, İlhan
Publicat a Mol Cytogenet (2015)