Search Results - Pierrottet, C O

  • Showing 1 - 3 results of 3
Refine Results
  1. 1
    Syndromic and non-syndromic forms of retinitis pigmentosa: a comprehensive Italian clinical and molecular study reveals new mutations

    Syndromic and non-syndromic forms of retinitis pigmentosa: a comprehensive Italian clinical and molecular study reveals new mutations by Pierrottet, C O, Zuntini, M, Digiuni, M, Bazzanella, I, Ferri, P, Paderni, R, Rossetti, L M, Cecchin, S, Orzalesi, N, Bertelli, M

    Get full text
    Items that cite this one
    Article
    Save to List
    Saved in:
  2. 2
    A novel spontaneous missense mutation in VMD2 gene is a cause of a Best macular dystrophy sporadic case

    A novel spontaneous missense mutation in VMD2 gene is a cause of a Best macular dystrophy sporadic case by Palomba, Grazia, Rozzo, Carla, Angius, Andrea, Pierrottet, Chiara O, Orzalesi, Nicola, Pirastu, Mario

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  3. 3
    CRB1 mutation spectrum in inherited retinal dystrophies

    CRB1 mutation spectrum in inherited retinal dystrophies by den Hollander, Anneke I., Davis, Jason, van der Velde-Visser, Saskia D., Zonneveld, Marijke N., Pierrottet, Chiara O., Koenekoop, Robert K., Kellner, Ulrich, van den Born, L. Ingeborgh, Heckenlively, John R., Hoyng, Carel B., Handford, Penny A., Roepman, Ronald, Cremers, Frans P.M.

    Published in Human mutation
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:

Search Tools: