Skip to
  1. Homepage
  2. Research and trials
  3. Registries & biobanks
Search by disease/gene

Search by disease/gene

*
(*) mandatory field




 

Other search option(s)

11 Result(s)

    • AUSTRIA
    • TIROL
    • INNSBRUCK
    • Austrian Country Node of the Human Variome Project (HVP)
    • Medizinische Universität Innsbruck
    • Sektion Humangenetik
    • More details
    • DENMARK
    • Sjælland
    • COPENHAGEN
    • Mendelian cytogenetics network online database
    • The Panum Institute-University of Copenhagen
    • Department of Cellular and Molecular Medicine
    • More details
    • ESTONIA
    • Tartu
    • TARTU
    • Biobank of the Estonian genome center
    • Tartu University Hospital
    • Centre of Genetics - United laboratories
    • More details
    • FRANCE
    • AUVERGNE
    • CLERMONT-FERRAND
    • Auvergne registry of congenital anomalies - contributes to the EUROCAT network
    • CHU de Clermont-Ferrand - Hôpital d'Estaing
    • Service de génétique
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • CLICHY
    • French patient registry affected by genetic deafness in France
    • CHU Paris Nord-Val de Seine - Hôpital Beaujon
    • Service d'oto-rhino-laryngologie
    • More details
    • GERMANY
    • Thüringen
    • JENA
    • Small supernumerary marker chromosomes (sSMC) registry
    • Universitätsklinikum Jena
    • Molekulare Zytogenetik (FISH Labor)
    • More details
    • MOROCCO
    • Rabat
    • RABAT
    • MoHuMuDa : Moroccan Human Mutation Database
    • Institut National d'Hygiène
    • Département de génétique médicale
    • More details
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • ECARUCA: cytogenetic and clinical database on rare chromosomal disorders
    • UMC St Radboud - Universitair Medisch Centrum St Radboud
    • Sectie Genoomdiagnostiek
    • More details
    • SPAIN
    • Madrid
    • MADRID
    • Registry of the Spanish Collaborative Study of Congenital Malformations (ECEMC)
    • Centro de Investigación sobre Anomalías Congénitas
    • More details
    • UNITED KINGDOM
    • Cambridgeshire
    • HINXTON
    • DECIPHER - database of chromosomal imbalance and phenotype in human using ensembl resources
    • Wellcome Trust Sanger Institute
    • DECIPHER
    • More details
    • UNITED KINGDOM
    • Greater Manchester
    • MANCHESTER
    • DMuDB: Diagnostic Mutation Database
    • St Mary's Hospital
    • National Genetics Reference Laboratory - Manchester
    • More details