Hasil Pencarian - Mahmoud R Fassad

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  1. 1
    CFAP300 mutation causing primary ciliary dyskinesia in Finland

    CFAP300 mutation causing primary ciliary dyskinesia in Finland oleh Rüdiger Schultz, Varpu Elenius, Mahmoud R. Fassad, Mahmoud R. Fassad, Grace Freke, Andrew Rogers, Amelia Shoemark, Amelia Shoemark, Tiina Koistinen, Mai A. Mohamed, Mai A. Mohamed, Jacqueline S. Y. Lim, Hannah M. Mitchison, Anu I. Sironen, Anu I. Sironen

    Diterbitkan 2022-09-01
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  2. 2
    CYP1B1 and myocilin gene mutations in Egyptian patients with primary congenital glaucoma

    CYP1B1 and myocilin gene mutations in Egyptian patients with primary congenital glaucoma oleh Mahmoud R. Fassad, Asmaa K. Amin, Heba A. Morsy, Noha M. Issa, Nader H. Bayoumi, Sahar A. El Shafei, Soha F. Kholeif

    Diterbitkan 2017-07-01
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  3. 3
    Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study

    Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study oleh Michelle Bisschoff, Izelle Smuts, Marli Dercksen, Maryke Schoonen, Barend C. Vorster, George van der Watt, Careni Spencer, Kireshnee Naidu, Franclo Henning, Surita Meldau, Robert McFarland, Robert W. Taylor, Krutik Patel, Mahmoud R. Fassad, Jana Vandrovcova, The ICGNMD Consortium, Ronald J. A. Wanders, Francois H. van der Westhuizen

    Diterbitkan 2024-01-01
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  4. 4
    The Palestinian primary ciliary dyskinesia population: first results of the diagnostic and genetic spectrum

    The Palestinian primary ciliary dyskinesia population: first results of the diagnostic and genetic spectrum oleh Nisreen Rumman, Mahmoud R. Fassad, Corine Driessens, Patricia Goggin, Nader Abdelrahman, Adel Adwan, Mutaz Albakri, Jagrati Chopra, Regan Doherty, Bishara Fashho, Grace M. Freke, Abdallah Hasaballah, Claire L. Jackson, Mai A. Mohamed, Reda Abu Nema, Mitali P. Patel, Reuben J. Pengelly, Ahmad Qaaqour, Bruna Rubbo, N. Simon Thomas, James Thompson, Woolf T. Walker, Gabrielle Wheway, Hannah M. Mitchison, Jane S. Lucas

    Diterbitkan 2023-04-01
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  5. 5
    Pathological variants in TOP3A cause distinct disorders of mitochondrial and nuclear genome stability

    Pathological variants in TOP3A cause distinct disorders of mitochondrial and nuclear genome stability oleh Direnis Erdinc, Alejandro Rodríguez‐Luis, Mahmoud R Fassad, Sarah Mackenzie, Christopher M Watson, Sebastian Valenzuela, Xie Xie, Katja E Menger, Kate Sergeant, Kate Craig, Sila Hopton, Gavin Falkous, Genomics England Research Consortium, Joanna Poulton, Hector Garcia‐Moreno, Paola Giunti, Carlos A deMoura Aschoff, Jonas A Morales Saute, Amelia J Kirby, Camilo Toro, Lynne Wolfe, Danica Novacic, Lior Greenbaum, Aviva Eliyahu, Ortal Barel, Yair Anikster, Robert McFarland, Gráinne S Gorman, Andrew M Schaefer, Claes M Gustafsson, Robert W Taylor, Maria Falkenberg, Thomas J Nicholls

    Diterbitkan 2023-05-01
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  6. 6
    X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3

    X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3 oleh Chiara Olcese, Mitali P. Patel, Amelia Shoemark, Santeri Kiviluoto, Marie Legendre, Hywel J. Williams, Cara K. Vaughan, Jane Hayward, Alice Goldenberg, Richard D. Emes, Mustafa M. Munye, Laura Dyer, Thomas Cahill, Jeremy Bevillard, Corinne Gehrig, Michel Guipponi, Sandra Chantot, Philippe Duquesnoy, Lucie Thomas, Ludovic Jeanson, Bruno Copin, Aline Tamalet, Christel Thauvin-Robinet, Jean- François Papon, Antoine Garin, Isabelle Pin, Gabriella Vera, Paul Aurora, Mahmoud R. Fassad, Lucy Jenkins, Christopher Boustred, Thomas Cullup, Mellisa Dixon, Alexandros Onoufriadis, Andrew Bush, Eddie M. K. Chung, Stylianos E. Antonarakis, Michael R. Loebinger, Robert Wilson, Miguel Armengot, Estelle Escudier, Claire Hogg, UK10K Rare Group, Serge Amselem, Zhaoxia Sun, Lucia Bartoloni, Jean-Louis Blouin, Hannah M. Mitchison

    Diterbitkan 2017-02-01
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