Hasil Pencarian - Hatice Mutlu

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  1. 1
    The Spectrum of NF1 Gene Variations in Southeastern Turkey

    The Spectrum of NF1 Gene Variations in Southeastern Turkey oleh Emre Kırat, Hatice Mutlu Albayrak

    Diterbitkan 2021-09-01
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  2. 2
    Fetal Valproate Syndrome

    Fetal Valproate Syndrome oleh Hatice Mutlu-Albayrak, Cahide Bulut, Hüseyin Çaksen

    Diterbitkan 2017-04-01
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  3. 3
    Yenidoğanda distal renal tübüler asidozisli Joubert Sendromu

    Yenidoğanda distal renal tübüler asidozisli Joubert Sendromu oleh Rahmi Örs, Hüseyin Çaksen, Hüseyin Altunhan, Hatice Mutlu, Nuriye Tarakçı

    Diterbitkan 2015-06-01
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  4. 4
    About the activity and selectivity of less well-known metathesis catalysts during ADMET polymerizations

    About the activity and selectivity of less well-known metathesis catalysts during ADMET polymerizations oleh Hatice Mutlu, Lucas Montero de Espinosa, Oĝuz Türünç, Michael A. R. Meier

    Diterbitkan 2010-12-01
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  5. 5
    Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect

    Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect oleh Hatice Mutlu-Albayrak, Judit Bene, Mehmet Burhan Oflaz, Tijen Tanyalçın, Hüseyin Çaksen, Bela Melegh

    Diterbitkan 2015-01-01
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  6. 6
    A GHOSAL HEMATODIAPHYSEAL DYSPLASIA CASE; EXCELLENT RESPONSE TO NON-STEROIDAL ANTI-INFLAMATORY DRUG TREATMENT

    A GHOSAL HEMATODIAPHYSEAL DYSPLASIA CASE; EXCELLENT RESPONSE TO NON-STEROIDAL ANTI-INFLAMATORY DRUG TREATMENT oleh Hasan Fatih Cakmaklı, Hatice Mutlu, Şule Altıner, Fatma Aydın, Talia Ilerı, Elif Ince, Mehmet Ertem

    Diterbitkan 2023-10-01
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  7. 7
    Evaluation of the Neurodevelopmental Status for Urea Cycle Disorders: Based on Clinical Experience

    Evaluation of the Neurodevelopmental Status for Urea Cycle Disorders: Based on Clinical Experience oleh Ayşe Ergül Bozacı, Emine Göksoy, Aysel Tekmenuray Ünal, Hatice Mutlu Albayrak, İbrahim Taş, Berat Kanar, Mehmet Nuri Özbek, Melis Köse

    Diterbitkan 2023-09-01
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  8. 8
    Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations

    Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations oleh Elisa Adele Colombo, Hatice Mutlu-Albayrak, Yousef Shafeghati, Mine Balasar, Juliette Piard, Davide Gentilini, Davide Gentilini, Anna Maria Di Blasio, Cristina Gervasini, Lionel Van Maldergem, Lidia Larizza

    Diterbitkan 2019-05-01
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