Vai a
  1. Homepage
  2. Ricerca e sperimen- tazioni
  3. Progetti di ricerca
Ricerca per malattia/gene

Ricerca per malattia/gene

*
(*) campo obbligatorio


 

Altre opzioni di ricerca

10 Risultato/i

Partnership : Accademici = Accademici 
, Industria = Industria 
, Investitori finanziari = Investitori finanziari

    • AUSTRIA
    • WIEN
    • WIEN
    • Screening for mutations in genes responsible for hearing impairment and their epidemiological relevance
    • Allgemeines Krankenhaus
    • Universitätsklinik für Hals-, Nasen- und Ohrenheilkunde
    • Ulteriori dettagli
    • CANADA
    • Colombie-Britannique
    • VANCOUVER
    • FORGE - Finding of Rare Disease Genes in Canada
    • University of British Columbia
    • Faculty of Medicine
    • Ulteriori dettagli
    • CANADA
    • Ontario
    • OTTAWA, ONTARIO
    • FORGE - Finding of Rare Disease Genes in Canada
    • University of Ottawa
    • Faculty of Medicine -
    • Ulteriori dettagli
    • CANADA
    • Québec
    • MONTREAL
    • FORGE - Finding of Rare Disease Genes in Canada
    • Centre hospitalier universitaire Sainte-Justine
    • Pédiatrie
    • Ulteriori dettagli
    • ESTONIA
    • Tartu
    • TARTU
    • The prevalence and genetic background of hereditary hearing impairment in Estonia
    • Children's Clinic of Tartu University
    • Department of Paediatrics
    • Ulteriori dettagli
    • FRANCIA
    • ILE-DE-FRANCE
    • CLICHY
    • Search for gene mutations in patients affected by genetic deafness
    • CHU Paris Nord-Val de Seine - Hôpital Beaujon
    • Service d'oto-rhino-laryngologie
    • Ulteriori dettagli
    • FRANCIA
    • ILE-DE-FRANCE
    • CRETEIL
    • Waardenburg syndroms molecular basis
    • GH Henri Mondor
    • Génétique moléculaire et développement
    • Ulteriori dettagli
    • FRANCIA
    • ILE-DE-FRANCE
    • PARIS
    • Characterization of new genes involved in non-syndromic and syndromic deafness (especially Usher syndrome) and corresponding impairement physiopathology
    • Institut Pasteur
    • Unité de Génétique et physiologie cellulaire
    • Ulteriori dettagli
    • ITALIA
    • LAZIO
    • ROMA
    • GENESKIN: European network on rare genetic skin diseases (coordination)
    • Istituto Dermopatico dell'Immacolata - IRCCS
    • Laboratorio di Biologia Molecolare e Cellulare
    • Ulteriori dettagli
    • ITALIA
    • VENETO
    • PADOVA
    • Meccanismi di patogenicita' e prospettive terapeutiche per la sordita' genetica associata a mutazioni di connessine
    • Venetian Institute of Molecular Medicine
    • Centro Interdipartimentale per lo Studio dei Segnali Cellulari
    • Ulteriori dettagli