Browsing by Author Zeybek, Selcan
Showing results 1 to 5 of 5
| Issue Date | Title | Author(s) |
|---|---|---|
| 2019 | The co-existence of Nablus Mask-Like Facial Syndrome and Klinefelter Syndrome | Anlaş, Özlem ; Sarikepe, B; Zeybek, Selcan; Özturk, Menekşe; Bağcı, Gülseren ; Çetin, Gökhan Ozan |
| 2017 | Familial mutation in caffey disease with reduced penetrance: A case report | Özdemir, Özmert Muhammet Ali ; Tancer-Elçi, Hazal; Polat, Aziz ; Güçtürk, İinci; Tepeli, Emre ; Zeybek, Selcan; Ayaz, Akif |
| 2019 | Further delineation of ACPHD syndrome and a novel mutation in DNAJC3 | Zeybek, Selcan; Farre, G; Öztürk, Menekşe ; Albuz, Burcu ; Beltran, S; Bowcock, A; Çetin, Gökhan Ozan |
| 2019 | A Novel Nonsense Mutation In The EYA1 Gene Found In A Patient With BOR Syndrome | Öztürk, Menekşe ; Zeybek, Selcan; Dursun, Belda ; Albuz, Burcu ; Anlas, Özlem; Gurkan, H; Çetin, Gökhan Ozan |
| 2015 | Tekrarlayan gebelik kaybı olan vakalarda pentraxin 3 ekspresyon profilinin belirlenmesi | Zeybek, Selcan |