. 2018; 35(3): 202-203 | DOI: 10.4274/tjh.2017.0385  

İntrakraniyal Kanama ile Başvuran Hemofili A Olgusu: Yeni Bir Mutasyonun Moleküler Olarak Tanımlanması

Burcak Tatlı Güneş1, Zühal Önder Siviş1, Eda Ataseven1, Barış Malbora1, Meral Türker1, Burcu Fatma Belen2, Berna Atabay1, Tahir Atik3, Esra Işık3, Ferda Özkınay3
1İzmir Tepecik Training and Research Hospital, Clinic of Pediatric Hematology, İzmir, Turkey
2Başkent University Faculty of Medicine, Department of Pediatric Hematology, Ankara, Turkey
3Ege University Faculty of Medicine, Department of Pediatric Genetics, İzmir, Turkey

Anahtar Kelimeler: Hemofili, İntrakraniyal kanama, Kız cinsiyet


Intracranial Bleeding in a Female Hemophilia Patient: Molecular Analysis of the Factor 8 Gene and Determination of a Novel Mutation

Burcak Tatlı Güneş1, Zühal Önder Siviş1, Eda Ataseven1, Barış Malbora1, Meral Türker1, Burcu Fatma Belen2, Berna Atabay1, Tahir Atik3, Esra Işık3, Ferda Özkınay3
1İzmir Tepecik Training and Research Hospital, Clinic of Pediatric Hematology, İzmir, Turkey
2Başkent University Faculty of Medicine, Department of Pediatric Hematology, Ankara, Turkey
3Ege University Faculty of Medicine, Department of Pediatric Genetics, İzmir, Turkey

Keywords: Hemophilia, Intracranial bleeding, Female


Burcak Tatlı Güneş, Zühal Önder Siviş, Eda Ataseven, Barış Malbora, Meral Türker, Burcu Fatma Belen, Berna Atabay, Tahir Atik, Esra Işık, Ferda Özkınay. Intracranial Bleeding in a Female Hemophilia Patient: Molecular Analysis of the Factor 8 Gene and Determination of a Novel Mutation. . 2018; 35(3): 202-203

Sorumlu Yazar: Burcu Fatma Belen, Türkiye


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