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9 matching term(s)

Funded by an IRDiRC member =

    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Pathophysiology of Vascular Anomalies and lymphedema
    • FRS-FNRS
    • Fonds de la Recherche Scientifique
    • More details
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUXELLES
    • Pathophysiology of Vascular Anomalies and lymphedema
    • Université Catholique de Louvain - UCL
    • Laboratory of Human Molecular Genetics
    • More details
    • BELGIUM
    • OOST-VLAANDEREN
    • GENT
    • Long-range genetic defects in human developmental conditons
    • Ghent University Hospital - UZGent
    • Center for Medical Genetics Ghent
    • More details
    • CANADA
    • Ontario
    • TORONTO
    • Funded by an IRDiRC member
    • Computerized Patient Phenotyping to Connect Canadian Clinical Genetics Clinics
    • University of Toronto
    • Department of Computer Science
    • More details
    • FRANCE
    • BOURGOGNE
    • DIJON
    • Funded by an IRDiRC member
    • MOSAIC: A genomic approach to identify postzygotic mutations in mosaic developmental diseases involving the skin
    • Université de Bourgogne
    • Faculté de Médecine
    • More details
    • ITALY
    • LAZIO
    • ROMA
    • GENESKIN: European network on rare genetic skin diseases (coordination)
    • Istituto Dermopatico dell'Immacolata - IRCCS
    • Laboratorio di Biologia Molecolare e Cellulare
    • More details
    • ITALY
    • PIEMONTE
    • TORINO
    • Cellular and animal models of CLOVES syndrome
    • Università degli Studi di Torino
    • Sezione di Neuroscienze
    • More details
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • Funded by an IRDiRC member
    • NIHR BioResource - Rare Disease: SPEED - Specialist Pathology: Evaluating Exomes in Diagnostics
    • Wellcome Trust/MRC Building
    • Cambridge Institute for Medical Research
    • More details
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • NIPSIGEN - Clinical translation of non-invasive prenatal diagnosis (NIPD) for single gene disorders (Health Innovation Challenge Fund)
    • Birmingham Women's NHS Foundation Trust
    • Regional Genetics Unit
    • More details