PROYECTOS DE INVESTIGACIÓN SOBRE ARTROGRIPOSIS MULTIPLE CONGÉNITA ABIERTOS EN DISTINTOS PAÍSES

- Molecular genetics and biology of lethal fetal arthrogryposes in Finland
- National Institute for Health and Welfare
- Kansantautien genetiikan yksikkö
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- FINLANDIA
- Finland
- HELSINKI
- Diagnosis of ARC – Arthrogryposis – renal dysfunction – cholestasis- syndrome (Mutation screening of the VIPAR and VPS33B genes)
- UCL University College London
- MRC Laboratory for Molecular Cell Biology
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- REINO UNIDO (EL)
- Greater London
- LONDON
- The Deciphering Developmental Disorders (the DDD study)
- Wellcome Trust Sanger Institute
- DECIPHER
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- REINO UNIDO (EL)
- Cambridgeshire
- HINXTON
- Exploring the Genetics of Renal Developmental Disease
- Royal Devon and Exeter Hospital – Wonford site
- Department of Urology
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- REINO UNIDO (EL)
- Devon
- EXETER
- Long-range genetic defects in human developmental conditons
- Ghent University Hospital – UZGent
- Center for Medical Genetics Ghent
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- BELGICA
- OOST-VLAANDEREN
- GENT
- Computerized Patient Phenotyping to Connect Canadian Clinical Genetics Clinics
- University of Toronto
- Department of Computer Science
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- CANADA
- Ontario
- TORONTO
- The policy of public health genomics in Italy
- IRCCS Ospedale Pediatrico Bambino Gesù – SEDE GIANICOLO
- Servizio Clinico di Consulenza Genetica
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- ITALIA
- LAZIO
- ROMA
- Study of improving Safety of Lentiviral Gene Transfer
- IRCCS Ospedale San Raffaele
- Centro di Genomica, Bioinformatica e Biostatistica – Unità di Genetica Umana e Molecolare
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- ITALIA
- LOMBARDIA
- MILANO
- Gene therapy strategies for Antigen-specific tolerance induction in vivo
- Istituto San Raffaele Telethon per la Terapia Genica – TIGET
- Unità di Ricerca Clinica Pediatrica
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- ITALIA
- LOMBARDIA
- MILANO
- NIHR BioResource – Rare Disease: SPEED – Specialist Pathology: Evaluating Exomes in Diagnostics
- Wellcome Trust/MRC Building
- Cambridge Institute for Medical Research
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- REINO UNIDO (EL)
- Cambridgeshire
- CAMBRIDGE
- 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
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- REINO UNIDO (EL)
- West Midlands
- BIRMINGHAM