Hasil Pencarian - Ebru Erzurumluoglu Gokalp

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  1. 1
    Association of eleven single nucleotide polymorphisms with refractive disorders from Eskisehir, Turkey

    Association of eleven single nucleotide polymorphisms with refractive disorders from Eskisehir, Turkey oleh Nadir Unlu, Ebru Erzurumluoglu Gokalp, Serap Arslan, Oguz Cilingir, Muzaffer Bilgin, Engin Yildirim, Huseyin Gursoy

    Diterbitkan 2021-06-01
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  2. 2
    Screening of Mutations in Maturity-onset Diabetes of the Young-related Genes and RFX6 in Children with Autoantibody-negative Type 1 Diabetes Mellitus

    Screening of Mutations in Maturity-onset Diabetes of the Young-related Genes and RFX6 in Children with Autoantibody-negative Type 1 Diabetes Mellitus oleh Enver Şimşek, Oğuz Çilingir, Tülay Şimşek, Sinem Kocagil, Ebru Erzurumluoğlu Gökalp, Meliha Demiral, Çiğdem Binay

    Diterbitkan 2024-06-01
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  3. 3
    Genetic variants associated with atrial fibrillationand long-term recurrence after catheter ablation for atrialfibrillation in Turkish patients

    Genetic variants associated with atrial fibrillationand long-term recurrence after catheter ablation for atrialfibrillation in Turkish patients oleh Taner Ulus, Muhammet Dural, Pelin Meşe, Furkan Yetmiş, Kadir Uğur Mert, Bülent Görenek, Oğuz Çilingir, Ebru Erzurumluoglu Gökalp, Serap Arslan, Sevilhan Artan, Özlem Aykaç, Ertuğrul Çolak, Hikmet Yorgun, Uğur Canpolat, Kudret Aytemir

    Diterbitkan 2021-02-01
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  4. 4
    Which prognostic marker is responsible for the clinical heterogeneity in CLL with 13q deletion?

    Which prognostic marker is responsible for the clinical heterogeneity in CLL with 13q deletion? oleh Beyhan Durak Aras, Sevgi Isik, Hava Uskudar Teke, Abdulvahap Aslan, Filiz Yavasoglu, Zafer Gulbas, Fatih Demirkan, Hulya Ozen, Oguz Cilingir, Nur Sena Inci, Gulcin Gunden, Tuba Bulduk, Ebru Erzurumluoglu Gokalp, Sinem Kocagil, Sevilhan Artan, Olga Meltem Akay

    Diterbitkan 2021-01-01
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