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Funded by an IRDiRC member =

    • BELGIUM
    • OOST-VLAANDEREN
    • GENT
    • Molecular genetic characterisation of defects in extracellular matrix microfibrils and their correlation with morphological and functional defects of the cardiovascular system.
    • Ghent University Hospital - UZGent
    • Center for Medical Genetics Ghent
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • MONTROUGE
    • Metalloproteinases expression in aortic and pulmonary artery walls and skin in conjonctivodysplasias
    • Faculté de chirurgie dentaire
    • Laboratoire de physiopathologie des tissus non minéralisés
    • More details
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Molecular and immunological investigation of the phenotypic overlap between Loeys-Dietz Syndrome and Autosomal dominant hyper IgE syndrome
    • CCI am Universitätsklinikum Freiburg
    • Centrum für Chronische Immundefizienz
    • More details
    • ITALY
    • LOMBARDIA
    • PAVIA
    • New genetic syndromes with aortic tortuosity and dissection
    • Fondazione IRCCS Policlinico San Matteo
    • Laboratorio di Diagnostica Molecolare, Patologia Cardiovascolare e dei Trapianti
    • More details
    • SWITZERLAND
    • Suisse Alémanique
    • SCHLIEREN
    • Molecular basis of Marfan syndrome and related disorders: Whole-exome sequencing and targeted therapy
    • Center for Cardiovascular Genetics and Gene Diagnostics
    • 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