Showing 1 - 10 results of 10 for search 'Koray Boduroğlu', query time: 0.02s Refine Results
  1. 1
    Celiac disease screening in 100 Turkish children with Down syndrome

    Celiac disease screening in 100 Turkish children with Down syndrome by Yasemin Alanay, Koray Boduroğlu, Ergül Tunçbilek

    Published 2005-04-01
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  2. 2
    A case of Sotos syndrome with 5q35 microdeletion and novel clinical findings

    A case of Sotos syndrome with 5q35 microdeletion and novel clinical findings by Esra Kılıç, Gülen Eda Utine, Koray Boduroğlu

    Published 2013-04-01
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  3. 3
    Analysis of MTHFR 1298A>C in addition to MTHFR 677C>T polymorphism as a risk factor for neural tube defects in the Turkish population

    Analysis of MTHFR 1298A>C in addition to MTHFR 677C>T polymorphism as a risk factor for neural tube defects in the Turkish population by Koray Boduroğlu, Yasemin Alanay, Mehmet Alikaşifoğlu, Dilek Aktaş, Ergül Tunçbilek

    Published 2005-10-01
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  4. 4
    Rare sex chromosome aneuploidies: 49,XXXXY and 48,XXXY syndromes

    Rare sex chromosome aneuploidies: 49,XXXXY and 48,XXXY syndromes by Pelin Ozlem Simşek, Gülen Eda Utine, Ayfer Alikaşifoğlu, Yasemin Alanay, Koray Boduroğlu, Nurgün Kandemir

    Published 2009-06-01
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  5. 5
    Jervell and Lange-Nielsen syndrome with homozygous missense mutation of the KCNQ1 gene

    Jervell and Lange-Nielsen syndrome with homozygous missense mutation of the KCNQ1 gene by Esra Kılıç, İlker Ertuğrul, Sema Özer, Mehmet Alikaşifoğlu, Dilek Aktaş, Koray Boduroğlu, Gülen Eda Ütine

    Published 2014-10-01
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  6. 6
    Subtelomeric rearrangements in mental retardation: Hacettepe University experience in 130 patients

    Subtelomeric rearrangements in mental retardation: Hacettepe University experience in 130 patients by Gülen Eda Utine, Tolga Celik, Yasemin Alanay, Mehmet Alikaşifoğlu, Koray Boduroğlu, Ergül Tunçbilek, Dilek Aktaş

    Published 2009-06-01
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  7. 7
    Hyaline fibromatosis syndrome: a rare, yet recognizable syndrome

    Hyaline fibromatosis syndrome: a rare, yet recognizable syndrome by Tuğba Daşar, Hasibe Nesligül Gönen, Kemal Kösemehmetoğlu, Özlem Tekşam, Koray Boduroğlu, Gülen Eda Utine, Pelin Özlem Şimşek Kiper

    Published 2024-05-01
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  8. 8
    Dermal fibroblast transcriptome indicates contribution of WNT signaling pathways in the pathogenesis of Apert syndrome

    Dermal fibroblast transcriptome indicates contribution of WNT signaling pathways in the pathogenesis of Apert syndrome by Arda Çetinkaya, Ekim Taşkıran, Tutku Soyer, Pelin Özlem Şimşek-Kiper, Gülen Eda Utine, Gökhan Tunçbilek, Koray Boduroğlu, Mehmet Alikaşifoğlu

    Published 2017-12-01
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  9. 9
    Clinical and molecular evaluation of 16 patients with Rett syndrome

    Clinical and molecular evaluation of 16 patients with Rett syndrome by Pınar Zengin-Akkuş, Ekim Z Taşkıran, Serkan Kabaçam, Pelin Özlem Şimşek-Kiper, Göknur Haliloğlu, Koray Boduroğlu, Gülen Eda Utine

    Published 2018-02-01
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  10. 10
    Non-immune hydrops fetalis: A retrospective analysis of 151 autopsies performed at a single center

    Non-immune hydrops fetalis: A retrospective analysis of 151 autopsies performed at a single center by Gözdem Kaykı, Gökçen Örgül, Gülen Eda Utine, Osman Koray Boduroğlu, Şule Yiğit, Murat Yurdakök, Beril Talim, Diclehan Orhan, Zuhal Akçören, Şafak Güçer, M Sinan Beksaç

    Published 2018-10-01
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