Hasil Pencarian - Hanife Saat

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  1. 1
    Expanding the genotype–phenotype correlations in Alport syndrome: novel mutations, digenic inheritance, and genetic modifiers

    Expanding the genotype–phenotype correlations in Alport syndrome: novel mutations, digenic inheritance, and genetic modifiers oleh Ibrahim Sahin, Nefise Kandemir, Hanife Saat

    Diterbitkan 2023-10-01
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  2. 2
    Novel Homozygous Variant in the SLC19A2 Gene Causing Thiamine Responsive Megaloblastic Anemia Syndrome: A Disease to Be Considered in Diabetes Clinics

    Novel Homozygous Variant in the SLC19A2 Gene Causing Thiamine Responsive Megaloblastic Anemia Syndrome: A Disease to Be Considered in Diabetes Clinics oleh Burak Canvar Helvacı, Hanife Saat, Sema Hepsen, Özant Helvacı, Erman Çakal

    Diterbitkan 2024-10-01
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  3. 3
    Molecular Approach of Hereditary Arrhythmias, Long QT Syndrome, and Arrhythmogenic Right Ventricular Cardiomyopathy

    Molecular Approach of Hereditary Arrhythmias, Long QT Syndrome, and Arrhythmogenic Right Ventricular Cardiomyopathy oleh Hanife Saat, Ibrahim Şahin, Haktan Bagğış Erdem, Senem Özgür, Semiha Terlemez Tokgöz, Taha Bahsi&775;

    Diterbitkan 2022-06-01
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  4. 4
    Presence of Multiple Endocrine Neoplasia-1 Mutations in Patients with Primary Hyperparathyroidism Detected on Clinical and Sonographical Suspicion: Report of 2 Novel Mutations

    Presence of Multiple Endocrine Neoplasia-1 Mutations in Patients with Primary Hyperparathyroidism Detected on Clinical and Sonographical Suspicion: Report of 2 Novel Mutations oleh Muhammet Cüneyt Bilginer, Cevdet Aydın, Sevgül Fakı, Oya Topaloğlu, Hanife Saat, Buşranur Çavdarlı, Reyhan Ersoy, Bekir Çakır

    Diterbitkan 2023-04-01
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