Search Results - Franco, Brunella

  • Showing 1 - 3 results of 3
Refine Results
  1. 1
    Cover Image

    A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation by Fukami, Maki (Author) , Kirsch, Stefan (Author) , Wöginger, Simone (Author) , Richter, Alexandra (Author) , Benes, Vladimir (Author) , Franco, Brunella (Author) , Muroya, Koji (Author) , Rao, Ercole (Author) , Merker, Sabine (Author) , Niesler, Beate (Author) , Ballabio, Andrea (Author) , Ansorge, Wilhelm (Author) , Ogata, Tsutomu (Author) , Rappold, Gudrun (Author) ,


    Get full text
    Article (Journal) Online Resource


    Saved in:
  2. 2
    Cover Image

    Mental retardation in a boy with an interstitial deletion at Xp22.3 involving STS, KAL1, and OA1: Implication for the MRX locus by Muroya, Koji (Author) , Ogata, Tsutomu (Author) , Matsuo, Nobutake (Author) , Nagai, Toshiro (Author) , Franco, Brunella (Author) , Ballabio, Andrea (Author) , Rappold, Gudrun (Author) , Sakura, Nobiro (Author) , Fukushima, Yoshimitsu (Author) ,


    Get full text
    Article (Journal) Online Resource


    Saved in:
  3. 3
    Cover Image

    A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy by Franco, Brunella (Author) , Meroni, Germana (Author) , Parenti, Giancarlo (Author) , Levilliers, Jacqueline (Author) , Bernard, Loris (Author) , Gebbia, Marinella (Author) , Cox, Liza (Author) , Maroteaux, Pierre (Author) , Sheffield, Leslie (Author) , Rappold, Gudrun (Author) , Andria, Generoso (Author) , Petit, Christine (Author) , Ballabio, Andrea (Author) ,


    Get full text
    Article (Journal) Online Resource


    Saved in:

Search Tools: