Browsing by Author Albuz, Burcu
Showing results 1 to 7 of 7
| Issue Date | Title | Author(s) |
|---|---|---|
| 2022 | Analysis of Differences in DNA Damage and Repair Efficacy in Lymphocytes of Patients with Bipolar Disorder | Mart, Gökçe ; Ateşci, Feride Figen ; Mart, Mehmet ; Seçme, Mücahit ; Dodurga, Yavuz ; Albuz, Burcu |
| 2019 | Co-existence of multiple subclones in ETV6/RUNX1 at diagnosis of B-cell lymphoblastic leukemia | Caner, Vildan ; Sen Türk, Nilay ; Çetin, Gökhan Ozan ; Albuz, Burcu ; Ay, Yılmaz |
| 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 |
| 2022 | A rare missense Duchenne muscular dystrophy gene variant in a family with muscular dystrophy from Turkey | Albuz, Burcu ; Erdoğan, Çağdaş ; Demiray, Aydın ; Akca, Hakan ; Tokgun, Onur |
| 2020 | Williams-Beuren Sendromlu Çocukların Klinik ve Ekokardiyografik Değerlendirilmesi | Gürses, Dolunay ; Kayakıran, Eda Didem ; Albuz, Burcu ; Çetin, G. Ozan |