Works matching IS 02681161 AND DT 2018 AND VI 33 AND IP 10


Results: 22
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    Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella.

    Published in:
    2018
    By:
    • Martinez, Guillaume;
    • Kherraf, Zine-Eddine;
    • Zouari, Raoudha;
    • Mustapha, Selima Fourati Ben;
    • Saut, Antoine;
    • Pernet-Gallay, Karin;
    • Bertrand, Anne;
    • Bidart, Marie;
    • Hograindleur, Jean Pascal;
    • Amiri-Yekta, Amir;
    • Fourati Ben Mustapha, Selima;
    • Kharouf, Mahmoud;
    • Karaouzène, Thomas;
    • Thierry-Mieg, Nicolas;
    • Dacheux-Deschamps, Denis;
    • Satre, Véronique;
    • Bonhivers, Mélanie;
    • Touré, Aminata;
    • Arnoult, Christophe;
    • Ray, Pierre F
    Publication type:
    journal article
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