Hasil Pencarian - Semra Gürsoy

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  1. 1
    Turner Syndrome and Its Variants

    Turner Syndrome and Its Variants oleh Semra Gürsoy, Derya Erçal

    Diterbitkan 2017-12-01
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  2. 2
    Three Siblings with Idiopathic Hypogonadotropic Hypogonadism in a Nonconsanguineous Family: A Novel KISS1R/GPR54 Loss-of-Function Mutation

    Three Siblings with Idiopathic Hypogonadotropic Hypogonadism in a Nonconsanguineous Family: A Novel KISS1R/GPR54 Loss-of-Function Mutation oleh Özlem Nalbantoğlu, Gülçin Arslan, Özge Köprülü, Filiz Hazan, Semra Gürsoy, Behzat Özkan

    Diterbitkan 2019-12-01
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  3. 3
    Autoimmunity and intestinal colonization by in patients with type 1 diabetes at the time of the diagnosis

    Autoimmunity and intestinal colonization by in patients with type 1 diabetes at the time of the diagnosis oleh Semra Gürsoy, Tuba Koçkar, Sezen Ugan Atik, Zerrin Önal, Hasan Önal, Erdal Adal

    Diterbitkan 2018-07-01
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  4. 4
    Spectrum of Clinical Manifestations in Turkish Patients with Williams-Beuren Syndrome: A Monocentric Study

    Spectrum of Clinical Manifestations in Turkish Patients with Williams-Beuren Syndrome: A Monocentric Study oleh Semra Gürsoy, Filiz Hazan, Cüneyt Zihni, Sezer Acar, Murat Muhtar Yılmazer, Timur Meşe, Behzat Özkan

    Diterbitkan 2021-09-01
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  5. 5
    A newborn with monosomy X in association with corpus callosum agenesis

    A newborn with monosomy X in association with corpus callosum agenesis oleh Duygu Onur Cura, Burcin Iscan, Semra Gursoy, Handan Guleryuz, Tufan Cankaya, Tulay Ozturk, Ozlem Giray Bozkaya

    Diterbitkan 2017-10-01
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  6. 6
    Detection of <italic>SHOX</italic> Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature

    Detection of <italic>SHOX</italic> Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature oleh Semra Gürsoy, Filiz Hazan, Ayça Aykut, Özlem Nalbantoğlu, Hüseyin Anıl Korkmaz, Korcan Demir, Behzat Özkan, Özgür Çoğulu

    Diterbitkan 2020-12-01
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  7. 7
    Genetic diagnosis of congenital hypopituitarism in Turkish patients by a target gene panel: novel pathogenic variants in GHRHR, GLI2, LHX4 and POU1F1 genes

    Genetic diagnosis of congenital hypopituitarism in Turkish patients by a target gene panel: novel pathogenic variants in GHRHR, GLI2, LHX4 and POU1F1 genes oleh Tarık Kırkgöz, Semra Gürsoy, Sezer Acar, Özlem Nalbantoğlu, Beyhan Özkaya, Hüseyin Anıl Korkmaz, Filiz Hazan, Behzat Özkan

    Diterbitkan 2023-11-01
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  8. 8
    A Null Mutation of TNFRSF11A Causes Dysosteosclerosis, Not Osteopetrosis

    A Null Mutation of TNFRSF11A Causes Dysosteosclerosis, Not Osteopetrosis oleh Tarık Kırkgöz, Behzat Özkan, Filiz Hazan, Sezer Acar, Özlem Nalbantoğlu, Beyhan Özkaya, Melike Ataseven Kulalı, Semra Gürsoy, Shiro Ikegawa, Long Guo

    Diterbitkan 2022-06-01
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  9. 9
    The effects of epigenetic regulation on phenotypic expressivity in Turkish patients with familial Mediterranean fever

    The effects of epigenetic regulation on phenotypic expressivity in Turkish patients with familial Mediterranean fever oleh Eser Dogan, Semra Gursoy, Giray Bozkaya, Secil Arslansoyu Camlar, Ozge Aksel Kilicarslan, Alper Soylu, Ayfer Ulgenalp, Salih Kavukcu, Ozlem Giray Bozkaya

    Diterbitkan 2019-01-01
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  10. 10
    Brucellosis impairs endothelial functions in chronic symptomatic patients without overt cardiac involvement

    Brucellosis impairs endothelial functions in chronic symptomatic patients without overt cardiac involvement oleh Mustafa Ozan Gürsoy, İrfan Tursun, Mehmet Alpua, Aslı Haykır Solay, Müge Tokat Çobanlı, Hale Demirtaş, Gülten Ercan, Semra Gürsoy, Macit Kalçık, Süleyman Karakoyun, Mehmet Özkan

    Diterbitkan 2015-04-01
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  11. 11
    Identification of PCDH19 gene mutations/deletions in patients with early onset epilepsy

    Identification of PCDH19 gene mutations/deletions in patients with early onset epilepsy oleh Semra Gursoy, Esra Ataman, Bahar Toklu Baysal, Berk Özyılmaz, Pınar Gençpınar, Ayşe Semra Hız, Uluç Yiş, Aycan Ünalp, Nihal Olgaç Dündar, Ayfer Ülgenalp, Derya Erçal

    Diterbitkan 2020-01-01
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  12. 12
    De Novo <i>PORCN</i> and <i>ZIC2</i> Mutations in a Highly Consanguineous Family

    De Novo <i>PORCN</i> and <i>ZIC2</i> Mutations in a Highly Consanguineous Family oleh Laura Castilla-Vallmanya, Semra Gürsoy, Özlem Giray-Bozkaya, Aina Prat-Planas, Gemma Bullich, Leslie Matalonga, Mónica Centeno-Pla, Raquel Rabionet, Daniel Grinberg, Susanna Balcells, Roser Urreizti

    Diterbitkan 2021-02-01
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