Browsing by Author
Zeybek, S.
Showing results 1 to 5 of 5
| Issue Date | Title | Author(s) |
| 2018 | Co-existence of goldenhar and klinefelter syndromes in a patient born following ICSI | Zeybek, S.; Sarıkepe, B.; Bağcı, Gülseren ; Alataş, E. ; Düzcan, F. |
| 2020 | Impending central retinal vein occlusion and cilioretinal artery occlusion in a pediatric case with MTHFR A1298C heterozygous polymorphism and ANA positivity | Kasikci, S.A.; Çetin, Ebru Nevin ; Parca, O. ; Pekel, Gökhan ; Zeybek, S.; Yüksel, Selçuk |
| 2019 | Increased expression of pentraxin 3 in placental tissues from patients with unexplained recurrent pregnancy loss | Zeybek, S.; Tepeli, E.; Çetin, Gökhan Ozan ; Caner, Vildan ; Şenol, Hande ; Yildirim, B.; Bağcı, Gülseren |
| 2020 | A novel nonsense mutation in CHST3 in a Turkish patient with spondyloepiphyseal dysplasia, Omani type | Albuz, B.; Çetin, Gökhan Ozan ; Özhan, Bayram ; Sarikepe, B.; Anlaş, Ö.; Öztürk, M.; Zeybek, S. |
| 2014 | The Roberts syndrome: A case report of an infant with valvular aortic stenosis and mutation in ESCO2 | Dogan, M.; Firinci, F.; Balci, Y.I.; Zeybek, S.; Özgürler, F.; Erdogan, I.; Varan, B. |
