Achondrogenesis type 2 in a newborn with a novel mutation on the COL2A1 gene
Dogan, P, Varal, IG, Gorukmez, O, Akkurt, MO, Akdag, A
Association between the catechol-o-methyltransferase val158met polymorphism with susceptibility and severity of carpal tunnel syndrome
Erkol İnal, E, Eroğlu, P, Görükmez, O, Özemri Sağ, Ş, Yakut, T
A novel mutation in a newborn baby leading to glycogen storage disease type Ia
Dorum, S, Gorukmez, O
An investigation of the COMT gene Val158Met polymorphism in patients admitted to the emergency department because of synthetic cannabinoid use
Nennicioglu, Y, Kaya, H, Eraybar, S, Atmaca, S, Gorukmez, O, Armagan, E