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    • CANADA
    • Ontario
    • OTTAWA, ONTARIO
    • Detection and simulation of femoroacetabular impingement
    • University of Ottawa
    • School of Electrical Engineering and Computer Science (EECS)
    • More details
    • FRANCE
    • AQUITAINE
    • BORDEAUX
    • Research for one gene involved in Goldenhar syndrome
    • CHU de Bordeaux-GH Pellegrin
    • Laboratoire Maladies Rares : Génétique et Métabolisme
    • More details
    • FRANCE
    • AQUITAINE
    • BORDEAUX
    • GOLDGEN: Identification and investigation of a gene involved in monogenic forms of Goldenhar syndrome
    • CHU de Bordeaux-GH Pellegrin
    • Laboratoire Maladies Rares : Génétique et Métabolisme
    • More details
    • FRANCE
    • RHONE-ALPES
    • BRON
    • ANI: Molecular characterization of apparently balanced chromosomal rearrangements by next-generation sequencing in 55 patients with intellectual disability and/or multiple congenital anomalies
    • CHU de Lyon HCL - GH Est
    • Laboratoire de cytogénétique constitutionnelle
    • More details
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • SKELNET - Skeletal Dysplasia Network (coordination)
    • Zentrum für Kinder- und Jugendmedizin Freiburg
    • Geschäftsstelle SKELNET e.V. - Sektion Pädiatrische Genetik
    • More details
    • GERMANY
    • Nordrhein-Westfalen
    • ESSEN
    • SKELNET : Chondrocyte specific genes as part of the signaling regulation of chondrocyte differentiation
    • Universität Duisburg-Essen
    • Abteilung Entwicklungsbiologie
    • More details
    • GERMANY
    • Nordrhein-Westfalen
    • ESSEN
    • FACE - Molecular and pathophysiological mechanism of oculo-auriculo-vertebral spectrum (subproject 2)
    • Universitätsklinikum Essen
    • Institut für Humangenetik
    • More details
    • ITALY
    • LAZIO
    • ROMA
    • Genomic diagnosis and classification of rare disorders with mental retardation using high throughput technologies
    • Istituto CSS-Mendel
    • Laboratorio Specializzato di Genetica Medica
    • More details
    • TURKEY
    • TURKEY
    • ANKARA
    • CRANIRARE: an integrated clinical and scientific approach for craniofacial malformations (partner No. 5)
    • Hacettepe university
    • Chemical Engineering and Bioengineering Departments
    • More details
    • TURKEY
    • TURKEY
    • ANKARA
    • CRANIRARE: an integrated clinical and scientific approach for craniofacial malformations (partner No. 3)
    • Hacettepe university
    • Department of genetic
    • More details
    • TURKEY
    • TURKEY
    • ISTANBUL
    • CRANIRARE: an integrated clinical and scientific approach for craniofacial malformations (partner No. 4)
    • Istanbul Universitesi
    • Department of medical genetic
    • More details
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • 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
    • Greater London
    • LONDON
    • Natural history and management in Skeletal Dysplasias
    • Great Ormond Street Hospital for Children, NHS Foundation Trust
    • Clinical Genetics
    • More details
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • ESDN: European Skeletal Dysplasia Network (coordination)
    • International Centre for Life
    • Institute of Genetic Medicine
    • 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