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Funded by an IRDiRC member = 
Research projects
UNITED KINGDOM
Avon
BRISTOL
Clinical and molecular genetics study of Thrombocytopenia-Absent radius syndrome
St Michael's Hospital
Department of Clinical Genetics
ITALY
LOMBARDIA
PAVIA
Improving diagnostic skills for inherited thrombocytopenias: identification of ''novel'' forms and characterization of ''classical'' forms to develop a DNA microchip
Fondazione IRCCS Policlinico San Matteo
Clinica Medica III
FRANCE
PROVENCE-ALPES-COTE D'AZUR
MARSEILLE
Input of a multidisciplinary management approach in announcing the diagnosis for young children with serious constitutional hemorrhagic disease and their families
CHU de Marseille - Hôpital de la Timone
Service d'Hématologie pédiatrique
CANADA
Ontario
OTTAWA, ONTARIO
Detection and simulation of femoroacetabular impingement
University of Ottawa
School of Electrical Engineering and Computer Science (EECS)
GERMANY
Mecklenburg-Vorpommern
GREIFSWALD
Clinical and genetic investigations of hereditary and acquired thrombocytopenia
Universitätsmedizin Greifswald
Abteilung Transfusionsmedizin
SWITZERLAND
Suisse Alémanique
BASEL
Massively parallel sequencing for gene discovery in lethal fetal disorders
Universitätsspital Basel
Abteilung für Medizinische Genetik
UNITED KINGDOM
Cambridgeshire
HINXTON
The Deciphering Developmental Disorders (the DDD study)
Wellcome Trust Sanger Institute
DECIPHER
UNITED KINGDOM
Tyne & Wear
NEWCASTLE UPON TYNE
ESDN: European Skeletal Dysplasia Network (coordination)
Newcastle upon Tyne Hospitals NHS Trust
Institute of Genetic Medicine
FRANCE
ILE-DE-FRANCE
PARIS
STaHR : Stimulation of Targeted Homologous Recombination for Gene Therapy - FR
Muséum National d'Histoire Naturelle
Laboratoire Structure et Instabilité des Génomes - INSERM U1154 - CNRS 7196
FRANCE
PAYS DE LA LOIRE
NANTES
FROGH : FRench Regional Origins in Genetics for Health - FR
Institut de Recherche en Santé - Université de Nantes
L'Institut du thorax - Inserm UMR 1087 / CNRS UMR 6291
ITALY
CAMPANIA
NAPOLI
Telethon Undiagnosed Disease Program - Revised Proposal
TIGEM - Telethon Institute of Genetics and Medicine
Genomic Medicine - Telethon Institute of Genetics and Medicine
ITALY
LOMBARDIA
MILANO
RBDD: Rare Bleeding Disorders Database network (coordination)
Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico
Laboratorio di Patologie Molecolari Applicate alla Clinica
UNITED KINGDOM
Cambridgeshire
CAMBRIDGE
NIHR BioResource - Rare Disease: BPD - Bleeding and Platelet Diseases
National Blood Service Center
Division of Transfusion Medicine, Department of Haematology
CANADA
Ontario
TORONTO
Inherited bone marrow failure syndromes: from genomic discoveries to biology
Hospital for Sick Children, Research Institute
Multicentric Research projects
- Universitätsklinikum Magdeburg A.ö.R
- MONZ - Fehlbildungsmonitoring Sachsen-Anhalt
- Faculty of of Life Sciences - University of Manchester
- Wellcome Trust Centre for Cell Matrix Research - B.3016
- University of British Columbia
- Maternal Infant Child and Youth Research Network
- Muséum National d'Histoire Naturelle
- Laboratoire Structure et Instabilité des Génomes - INSERM U1154 - CNRS 7196
- Institut de Recherche en Santé - Université de Nantes
- L'Institut du thorax - Inserm UMR 1087 / CNRS UMR 6291
- IRCCS Ospedale Pediatrico Bambino Gesù - SEDE GIANICOLO
- Servizio Clinico di Consulenza Genetica
GERMANY
Sachsen-Anhalt
MAGDEBURG
International Clearinghouse for Birth Defects Monitoring Systems
UNITED KINGDOM
Greater Manchester
MANCHESTER
ESDN: European Skeletal Dysplasia Network
CANADA
Colombie-Britannique
VANCOUVER
Maternal Infant Child and Youth Research Network (MICYRN)
FRANCE
ILE-DE-FRANCE
PARIS
STaHR : Stimulation of Targeted Homologous Recombination for Gene Therapy
FRANCE
PAYS DE LA LOIRE
NANTES
FROGH : FRench Regional Origins in Genetics for Health
ITALY
LAZIO
ROMA