Rezultaty - Şükrü Palanduz

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  1. 1
    Genetic insights into non-obstructive azoospermia: Implications for diagnosis and TESE outcomes

    Genetic insights into non-obstructive azoospermia: Implications for diagnosis and TESE outcomes od Shahrashoub Sharifi, Murat Dursun, Ayla Şahin, Serdar Turan, Ayşe Altun, Özden Özcan, Arif Kalkanlı, Kıvanç Çefle, Şükrü Öztürk, Şükrü Palanduz, Ateş Kadıoğlu

    Wydane 2025
    Dokumenty pełnotekstowe
    Artigo
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  2. 2
    Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes

    Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes od Seval Türkmen, Gabriele Gillessen‐Kaesbach, Peter Meinecke, Beate Albrecht, Luitgard M. Neumann, V. Hesse, Şükrü Palanduz, S. Balg, Frank Majewski, Sigrun Fuchs, Petra Zschieschang, M. Greiwe, K. Mennicke, Friedmar R. Kreuz, Harald J Dehmel, Burkhard Rodeck, Jürgen Kunze, Sigrid Tinschert, Stefan Mundlos, Denise Horn

    Wydane 2003
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
    Artigo
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  3. 3
    REST Final-Exon-Truncating Mutations Cause Hereditary Gingival Fibromatosis

    REST Final-Exon-Truncating Mutations Cause Hereditary Gingival Fibromatosis od Yavuz Bayram, Janson J. White, Nursel Elçioğlu, Megan T. Cho, Neda Zadeh, Asuman Gedikbaşı, Şükrü Palanduz, Şükrü Öztürk, Kıvanç Çefle, Özgür Kasapçopur, Zeynep Coban‐Akdemir, Davut Pehli̇van, Amber Begtrup, Claudia M.B. Carvalho, Ingrid S. Paine, Ali Menteş, Kıvanç Bektaş Kayhan, Ender Karaca, Shalini N. Jhangiani, Donna M. Muzny, Richard A. Gibbs, James R. Lupski

    Wydane 2017
    Dokumenty pełnotekstowe
    Artigo
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  4. 4
    Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction

    Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction od Elena Bonora, Francesca Bianco, Lina Cordeddu, Michael J. Bamshad, Ludmila Francescatto, Dustin Dowless, Vincenzo Stanghellini, Rosanna Cogliandro, Greger Lindberg, Zeynel Mungan, Kıvanç Çefle, Tayfun Özçelık, Şükrü Palanduz, Şükrü Öztürk, Asuman Gedikbaşı, Alessandra Gori, Tommaso Pippucci, Claudio Graziano, Umberto Volta, Giacomo Caio, Giovanni Barbara, Mauro D’Amato, Marco Seri, Nicholas Katsanis, G. Cara Romeo, Roberto De Giorgio

    Wydane 2015
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
    Artigo
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  5. 5
    <i>WRN</i>Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects

    <i>WRN</i>Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects od Koutaro Yokote, Sirisak Chanprasert, Lin Lee, Katharina Eirich, Minoru Takemoto, Aki Watanabe, Naoko Koizumi, Davor Lessel, Takayasu Mori, Fuki M. Hisama, Paula D. Ladd, Brad Angle, Hagit Baris, Kıvanç Çefle, Şükrü Palanduz, Şükrü Öztürk, Antoinette Chateau, Kentaro Deguchi, T.K.M Easwar, Antonio Federico, Amy Fox, Theresa A. Grebe, Beverly N. Hay, Sheela Nampoothiri, Karen Seiter, Elizabeth A. Streeten, Raúl E. Piña-Aguilar, Gemma Poke, Martin Poot, Renata Posmyk, George M. Martin, Christian Kubisch, Detlev Schindler, Junko Oshima

    Wydane 2016
    Dokumenty pełnotekstowe
    Revisão
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