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Ricerca per malattia/gene

Ricerca per malattia/gene

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7 Risultato/i

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

    • BELGIO
    • ANTWERPEN
    • ANTWERPEN-EDEGEM
    • Genetics of monogenic forms of deafness
    • University and University Hospital of Antwerp
    • Centre of Medical Genetics
    • Ulteriori dettagli
    • DANIMARCA
    • Sjælland
    • COPENHAGEN
    • Genetic causes of syndromic and non-syndromic hearing impairement
    • Bispebjerg hospital
    • Department of audiology
    • Ulteriori dettagli
    • ESTONIA
    • Tartu
    • TARTU
    • The prevalence and genetic background of hereditary hearing impairment in Estonia
    • Tartu University Hospital
    • Department of Pediatrics
    • Ulteriori dettagli
    • FRANCIA
    • ILE DE FRANCE
    • PARIS
    • Epidémiologie, phénotypage et génotypage des surdités
    • Institut Pasteur
    • Unité de Génétique et physiologie cellulaire
    • Ulteriori dettagli
    • GERMANIA
    • Nordrhein-Westfalen
    • KÖLN
    • Genetische Ursachen des Hörverlustes
    • Klinikum der Universität zu Köln
    • Institut für Humangenetik
    • Ulteriori dettagli
    • REGNO UNITO; GRAN BRETAGNA
    • Greater London
    • LONDON
    • Etiology in syndromal and isolated deafness
    • Great Ormond Street Hospital for Children
    • NE Thames Regional Genetics Service
    • Ulteriori dettagli
    • SPAGNA
    • Madrid
    • MADRID
    • Sorderas genéticas: patogénesis molecular y epidemiología
    • Hospital Universitario Ramón y Cajal
    • Unidad de Genética Molecular
    • Ulteriori dettagli
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