Browsing by Author Öztürk, Menekşe
Showing results 1 to 4 of 4
| 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 |
| 2019 | Fetus with partial trisomy 4 and t(2;16) due to maternal complex rearrangement involving three chromosomes: a case report | Albuz, Burcu ; Çetin, Gökhan Ozan ; Özturk, Menekşe ; Caner, Vildan ; Gunduz, CNS; Bağcı, Gülseren |
| 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 |