Hasil Pencarian - Öztürk Özdemir

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  1. 1
    Aerodynamic Optimization of a UAV Wing subject to Weight, Geometric, Root Bending Moment, and Performance Constraints

    Aerodynamic Optimization of a UAV Wing subject to Weight, Geometric, Root Bending Moment, and Performance Constraints oleh Durmuş Sinan Körpe, Öztürk Özdemir Kanat

    Diterbitkan 2019-01-01
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  2. 2
    Warfarin Resistance: A Case Report

    Warfarin Resistance: A Case Report oleh Uğur Gönlügür, Tanseli Gönlügür, Öztürk Özdemir, Fatma Sılan

    Diterbitkan 2019-03-01
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  3. 3
    The diagnostic accuracy of non-invasive fetal RhD genotyping by using cell-free fetal DNA in maternal plasma

    The diagnostic accuracy of non-invasive fetal RhD genotyping by using cell-free fetal DNA in maternal plasma oleh Sinem Yalcintepe, Fatma Silan, Ozturk Ozdemir, Cisem Akurut

    Diterbitkan 2019-03-01
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  4. 4
    Association of endothelial nitric oxide synthase Glu298Asp gene polymorphism in psoriasis cases with hypertension

    Association of endothelial nitric oxide synthase Glu298Asp gene polymorphism in psoriasis cases with hypertension oleh Zerrin Ogretmen, Meliha Merve Hiz, Fatma Silan, Ahmet Uludag, Ozturk Ozdemir

    Diterbitkan 2014-07-01
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  5. 5
    Macular and choroidal thickness of children with Familial Mediterranean Fever gene mutation

    Macular and choroidal thickness of children with Familial Mediterranean Fever gene mutation oleh Fatih Battal, Hakan Aylanc, Yeliz Ekim, Fatma Silan, Sule Yildirim, Ozturk Ozdemir

    Diterbitkan 2018-04-01
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  6. 6
    Delayed time of atrial conduction in children with Familial Mediterranean Fever

    Delayed time of atrial conduction in children with Familial Mediterranean Fever oleh Fatih Battal, Şule Yıldırım, Hakan Aylanc, Nazan Kaymaz, Öztürk Özdemir, Fatih Binnetoglu

    Diterbitkan 2021-05-01
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  7. 7
    Two candidate genes for recurrent pregnancy loss and infertility: Could ZP3 and UPK3B give us new diagnostic and therapeutic approach?

    Two candidate genes for recurrent pregnancy loss and infertility: Could ZP3 and UPK3B give us new diagnostic and therapeutic approach? oleh Fatma Sılan, Baris Paksoy, Taner Karakaya, Onur Yildiz, Mine Urfali, Ozturk Ozdemir

    Diterbitkan 2017-08-01
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  8. 8
    Blau syndrome with a rare mutation in exon 9 of NOD2 gene

    Blau syndrome with a rare mutation in exon 9 of NOD2 gene oleh Jelena Velickovic, Fatma Silan, Firdevs Dincsoy Bir, Coskun Silan, Burcu Albuz, Ozturk Ozdemir

    Diterbitkan 2019-11-01
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  9. 9
    The clinical, cytogenetics and molecular characterization of inverted duplication/deletion of chromosome 8p in a boy with mental and motor retardation: Genotype-phenotype correlation in a case report

    The clinical, cytogenetics and molecular characterization of inverted duplication/deletion of chromosome 8p in a boy with mental and motor retardation: Genotype-phenotype correlati... oleh Fatma Silan, Romyla Bourouba, Taner Karakaya, Onur Yildiz, Baris Paksoy, Mine Urfali, Ozturk Ozdemir

    Diterbitkan 2018-10-01
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  10. 10
    The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas

    The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas oleh Hande Küçük Kurtulgan, Emine Elif Altuntaş, Malik Ejder Yıldırım, Öztürk Özdemir, Binnur Bağcı, İlhan Sezgin

    Diterbitkan 2019-12-01
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  11. 11
    Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia

    Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia oleh Malik Ejder Yildirim, Hande Kucuk Kurtulgan, Ozturk Ozdemir, Hasan Kilicgun, Didem S. Aydemir, Burak Baser, Ilhan Sezgin

    Diterbitkan 2019-12-01
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