Browsing by Author Çetin, Gökhan Ozan
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Issue Date | Title | Author(s) |
---|---|---|
2001 | 1997-1999 yılları arasında Pamukkale Üniversitesi Eğitim Uygulama ve Araştırma Hastanesi'nde doğan bebeklerde konjenital malformasyon sıklığı | Düzcan, Füsun ; Kılıç, İlknur ; Zincir, Mehmet; Çetin, G. Ozan |
2019 | Altered microRNA 5692b and microRNA let-7d expression levels in children and adolescents with attention deficit hyperactivity disorder | Aydin, S.U.; Kabukçu Başay, Bürge ; Çetin, Gökhan Ozan ; Güngör Aydın, Ayşegül ; Tepeli, E. |
2020 | A case of recombinant chromosome 4: further delineation of the clinical features | Anlaş, Özlem ; Çetin, G. Ozan ; Yararbaş, Kanay; Düzcan, Füsun ; Gündüz, Cavidan Nur Semerci; Ayaz, Akif ; Bağcı, Gülseren |
2009 | A case of schizophrenia accompanying velocardiofacial syndrome | Şengül, Cem ; Efe, Muharrem ; Tepeli, Emre ; Çetin, Gökhan Ozan ; Düzcan, Füsun ; Herken, Hasan |
2023 | The clinical phenotype of Koolen-de Vries syndrome in Turkish patients and literature review | Karamık, Gökçen; Tüysüz, Beyhan; Işık, Esra; Yılmaz, Ayşegül ; Alanay, Yasemin; Çiftçi Sunamak, Evrim; Durmusalioglu, Enise Avcı; Ozkinay, Ferda; Cetin, Gokhan Ozan ; Ozturk, Nuray; Mihci, Ercan |
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 | 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 |
2011 | Congenital arterial thrombosis in newborn: A case report | Özdemir, Özmert M.A. ; Kılıç, İlknur ; Küçüktaşçı, Kazım ; Gürses, Dolunay ; Karaca, Abdullah ; Oto, Murat ; Çetin, Gökhan Ozan |
2014 | Correlation of O6-Methylguanine DNA methyltransferase promoter methylation and clinicopathological parameters in bladder cancer | Çetin, Gökhan Ozan ; Caner, Vildan ; Türk, Nilay Şen ; Okur, V.; Can, O.; Eskicorapci, S.; Tuncay, L. |
2003 | Cytogenetic studies in patients with reproductive failure | Düzcan, Füsun ; Atmaca, Münevver; Çetin, Gökhan Ozan ; Bağcı, Hüseyin |
2012 | The determination of relationship between "excision repair cross-complementing group 1" (ERCC1) gene T19007C and C8092A single nucleotide polymorphisms and clinicopathological parameters in non-small cell lung cancer | Koç, Esin; Caner, Vildan ; Büyükpınarbaşılı, N.; Tepeli, Emre ; Türk, Nilay Şen ; Çetin, Gökhan Ozan ; Bağcı, Gülseren |
2023 | Diagnostic and Management Strategies of Bietti Crystalline Dystrophy: Current Perspectives | Saatçi, Ali Osman; Ataş, Ferdane; Çetin, Gökhan Ozan ; Kayabaşı, Mustafa |
2018 | Diffüz Büyük B-hücreli Lenfoma Patogenezinde Tümör-kökenli Ekzozomların Fonksiyonal Önemi | Bağcı, Gülseren ; Çetin, Gökhan Ozan ; Tepeli, Emre ; Türk, Nilay Şen ; Caner, Vildan |
2022 | Dominant Optik Atrofi | Çetin, Ebru Nevin ; Ün, Emine Şeker ; Çetin, G. Ozan |
2015 | Downregulation of VANGL1 inhibits cellular invasion rather than cell motility in hepatocellular carcinoma cells without stimulation | Çetin, Gökhan Ozan ; Toylu, Aslı; Atabey, Neşe; Sercan, Zeynep; Sakızlı, Meral |
2022 | Early onset disease, anarthria, areflexia, and dystonia can be the distinctive features of SPG64, a very rare form of hereditary spastic paraplegias | Olmez, Akgun; Cetin, Gokhan Ozan ; Karaer, Kadri |
2024 | Evaluation of the patients with the diagnosis of pontocerebellar hypoplasia: a multicenter national study | Çavuşoğlu, Dilek; Öztürk, Gülten; Türkdoğan, Dilşad; Hız Kurul, Semra; Yis, Uluç; Komur, Mustafa; İncecik, Faruk; Kara, Bulent; Sahin, Turkan; Unver, Olcay; Dilber, Cengiz; Mert, Gulen Gul; Gunay, Cagatay; Uzan, Gamze Sarikaya; Ersoy, Ozlem; Oktay, Yavuz; Mermer, Serdar; Tuncer, Gokcen Oz; Gungor, Olcay ; Ozcora, Gul Demet Kaya; Gumus, Ugur; Sezer, Ozlem; Cetin, Gokhan Ozan ; Demir, Fatma; Yilmaz, Arzu; Gurbuz, Gurkan; Topcu, Meral; Topaloglu, Haluk; Ceylan, Ahmet Cevdet; Ceylaner, Serdar; Gleeson, Joseph G.; Icagasioglu, Dilara Fusun; Sonmez, F. Mujgan |
2023 | Expanding the clinical and molecular features of tricho- rhino-phalangeal syndrome with a novel variant | Öztürk, Nuray; Karamık, Gökçen; Mutlu, Hatice; Yılmaz Bayer, Öznur; Mihci, Ercan; Çetin, Gökhan Ozan ; Nur, Banu |
2011 | Expression and amplification of topoisomerase-2? in type 1 and type 2 papillary renal cell carcinomas and its correlation with HER2/neu amplification | Düzcan, Füsun ; Duzcan, S.E.; Sen, S.; Yorukoglu, K.; Caner, Vildan ; Şen Türk, Nilay ; Çetin, Gökhan Ozan |
2020 | Expression and DNA methylation profiles of EZH2-target genes in plasma exosomes and matched primary tumor tissues of the patients with diffuse large B-cell lymphoma | Barış, İkbal Cansu; Hacıoğlu, Sibel ; Türk, Nilay Şen ; Çetin, Gökhan Ozan ; Zencır, S.; Bağcı, Gülseren ; Caner, Vildan |