Showing 1 - 3 results of 3 for search 'Estivill Xavier', query time: 0.02s Refine Results
  1. 1
    <it>MRPS18CP2 </it>alleles and <it>DEFA3 </it>absence as putative chromosome 8p23.1 modifiers of hearing loss due to mtDNA mutation A1555G in the 12S rRNA gene

    <it>MRPS18CP2 </it>alleles and <it>DEFA3 </it>absence as putative chromosome 8p23.1 modifiers of hearing loss due to mtDNA mutation A1555G in the 12S rRNA gene by Fischel-Ghodsian Nathan, Mercader Josep, Ballana Ester, Estivill Xavier

    Published 2007
    Connect to this object online.
    Book
    Save to List
    Saved in:
  2. 2
    BAC array CGH in patients with Velocardiofacial syndrome-like features reveals genomic aberrations on chromosome region 1q21.1

    BAC array CGH in patients with Velocardiofacial syndrome-like features reveals genomic aberrations on chromosome region 1q21.1 by Estivill Xavier, Gabau Elisabeth, García-Aragonés Manel, Heine Damià, Rosell Jordi, Armengol Lluís, Brunet Anna, Guitart Miriam

    Published 2009
    Connect to this object online.
    Book
    Save to List
    Saved in:
  3. 3
    A pooling-based genome-wide analysis identifies new potential candidate genes for atopy in the European Community Respiratory Health Survey (ECRHS)

    A pooling-based genome-wide analysis identifies new potential candidate genes for atopy in the European Community Respiratory Health Survey (ECRHS) by Kogevinas Manolis, Ramon González Juan, Bustamante Mariona, Castro-Giner Francesc, Jarvis Deborah, Heinrich Joachim, Antó Josep-Maria, Wjst Matthias, Estivill Xavier, de Cid Rafael

    Published 2009
    Connect to this object online.
    Book
    Save to List
    Saved in:

Search Tools: