Showing 1 - 3 results of 3 for search 'S. Odent', query time: 0.01s Refine Results
  1. 1
    A new syndromic case of hearing loss and ectodermal anomalies associated with a recurrent missense variation in GJB6 gene

    A new syndromic case of hearing loss and ectodermal anomalies associated with a recurrent missense variation in GJB6 gene by Badreddine Elmakhzen, Paul Rollier, Clémence Saillard, Benoit Godey, Cédric Le Marechal, Paul Gueguen, Isabelle Fajardy, Sylvie Odent, Laurent Pasquier

    Published 2025-05-01
    Get full text
    Article
    Save to List
    Saved in:
  2. 2
    The recurrent p.Glu3Lys variant in EHHADH is responsible for Fanconi syndrome with early liver dysfunction and mitochondrial abnormalities

    The recurrent p.Glu3Lys variant in EHHADH is responsible for Fanconi syndrome with early liver dysfunction and mitochondrial abnormalities by P. Rollier, A. Cospain, M. Barth, V. Milon, N. Gueguen, C. Homedan, V. Desquiret, C. Bris, E. Colin, L. Damaj, A. Ryckewaert, P. Reynier, S. Odent, P. Amati-Bonneau, V. Procaccio, D. Bonneau, A. Ziegler

    Published 2025-06-01
    Get full text
    Article
    Save to List
    Saved in:
  3. 3
    Optimizing care for MRKH patients: From malformation screening to uterus transplantation eligibility

    Optimizing care for MRKH patients: From malformation screening to uterus transplantation eligibility by Auriane Cospain, Ludivine Dion, Maud Bidet, Krystel Nyangoh Timoh, Chloé Quelin, Isis Carton, Alinoe Lavillaureix, Karine Morcel, Paul Rollier, Laurent Pasquier, Bénédicte Nouyou, Sylvie Odent, Daniel Guerrier, Erika Launay, Marc‐Antoine Belaud Rotureau, Mélanie Fradin, Sylvie Jaillard, Vincent Lavoué

    Published 2025-03-01
    Get full text
    Article
    Save to List
    Saved in:

Search Tools: