Search Results - Kose, Canan Ceylan

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  1. 1
    Anemia and thrombocytopenia due to a novel BRPF1 variant in a family from Çanakkale with intellectual disability and dysmorphic facies: Case report and review of the literature

    Anemia and thrombocytopenia due to a novel BRPF1 variant in a family from Çanakkale with intellectual disability and dysmorphic facies: Case report and review of the literature by Kose, Canan Ceylan, Kaya, Derya, Akcan, Mehmet Berkay, Silan, Fatma

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  2. 2
    A case report of a patient with neurodevelopmental disorder with impaired speech and hyperkinetic movements: A biallelic variant in the ZNF142 gene

    A case report of a patient with neurodevelopmental disorder with impaired speech and hyperkinetic movements: A biallelic variant in the ZNF142 gene by Kaya, Derya, Ceylan Köse, Canan, Akcan, Mehmet Berkay, Silan, Fatma

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  3. 3
    Spinal muscular atrophy carrier screening program: awareness and attitude of healthcare professionals in Turkey

    Spinal muscular atrophy carrier screening program: awareness and attitude of healthcare professionals in Turkey by Celik, Kubra Muge, Kose, Canan Ceylan, Kaya, Derya, Tekin, Koray, Silan, Fatma

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  4. 4
    CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow

    CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow by Kim, Angelina Haesoo, Sakin, Irmak, Viviano, Stephen, Tuncel, Gulten, Aguilera, Stephanie Marie, Goles, Gizem, Jeffries, Lauren, Ji, Weizhen, Lakhani, Saquib A, Kose, Canan Ceylan, Silan, Fatma, Oner, Sukru Sadik, Kaplan, Oktay I, Ergoren, Mahmut Cerkez, Mishra-Gorur, Ketu, Gunel, Murat, Sag, Sebnem Ozemri, Temel, Sehime G, Deniz, Engin

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