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Funded by an IRDiRC member =

    • 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
    • DENMARK
    • Nordjylland
    • AALBORG
    • Evaluation of the clinical service provided in a Greek Department of Genetics, in the field of rare dysmorphic syndromes
    • Aarhus Universitetshospital - Aalborg
    • Department of clinical genetics
    • More details
    • FINLAND
    • Finland
    • TURKU
    • Development of practical diagnostics of rare syndromes: Sotos, Charge
    • University of Turku
    • Department of Medical Biochemistry and Genetics
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular basis of statural advance in Sotos syndrome
    • CHU Paris - Hôpital Necker-Enfants Malades
    • Laboratoire de Génétique Moléculaire
    • More details
    • GERMANY
    • Thüringen
    • JENA
    • Collection and characterisation of cases with a small supernumerary marker chomosome with the goal of a genotype phenotype correlation
    • Institut für Humangenetik am Universitätsklinikum Jena
    • Molekulare Zytogenetik (FISH Labor)
    • More details
    • PORTUGAL
    • NORTE
    • PORTO
    • Integrated Micro-Nano-OPTO Fluidic systems for high-content diagnosis and studies of rare cancer cells
    • Instituto de Patologia e Imunologia Molecular da Universidade do Porto
    • Genética de Tumores
    • More details
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • Chromosomal anomaly
    • Karolinska University Hospital - Clinical Genetics
    • Clinical Genetics
    • More details
    • SWITZERLAND
    • Suisse Alémanique
    • SCHLIEREN
    • Identification of novel autosomal genes causing mental retardation
    • Universität Zürich
    • Institut für Medizinische Genetik
    • More details
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • ISO - Investigation of Segmental Overgrowth
    • Addenbrooke's Hospital
    • University of Cambridge Metabolic Research Laboratories
    • More details
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • Funded by an IRDiRC member
    • NIHR BioResource - Rare Disease: MPMT - Multiple primary malignant tumours
    • Addenbrooke's Hospital
    • Academic Department of Medical Genetics
    • 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
    • Cambridgeshire
    • HINXTON
    • The Deciphering Developmental Disorders (the DDD study)
    • Wellcome Trust Sanger Institute
    • DECIPHER
    • More details
    • UNITED KINGDOM
    • Devon
    • EXETER
    • Exploring the Genetics of Renal Developmental Disease
    • Royal Devon and Exeter Hospital - Wonford site
    • Department of Urology
    • 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