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11 Result(s)
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- Austrian Country Node of the Human Variome Project (HVP)
- Medizinische Universität Innsbruck
- Sektion Humangenetik
- More details
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- DENMARK
- Sjælland
- COPENHAGEN
- Mendelian cytogenetics network online database
- The Panum Institute-University of Copenhagen
- Department of Cellular and Molecular Medicine
- More details
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- Biobank of the Estonian genome center
- Tartu University Hospital
- Centre of Genetics - United laboratories
- More details
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- FRANCE
- AUVERGNE
- CLERMONT-FERRAND
- Auvergne registry of congenital anomalies - contributes to the EUROCAT network
- CHU de Clermont-Ferrand - Hôpital d'Estaing
- Service de génétique
- More details
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- FRANCE
- ILE-DE-FRANCE
- CLICHY
- French patient registry affected by genetic deafness in France
- CHU Paris Nord-Val de Seine - Hôpital Beaujon
- Service d'oto-rhino-laryngologie
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- Small supernumerary marker chromosomes (sSMC) registry
- Universitätsklinikum Jena
- Molekulare Zytogenetik (FISH Labor)
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- MoHuMuDa : Moroccan Human Mutation Database
- Institut National d'Hygiène
- Département de génétique médicale
- More details
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- NETHERLANDS
- Gelderland
- NIJMEGEN
- ECARUCA: cytogenetic and clinical database on rare chromosomal disorders
- UMC St Radboud - Universitair Medisch Centrum St Radboud
- Sectie Genoomdiagnostiek
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- Registry of the Spanish Collaborative Study of Congenital Malformations (ECEMC)
- Centro de Investigación sobre Anomalías Congénitas
- More details
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- UNITED KINGDOM
- Cambridgeshire
- HINXTON
- DECIPHER - database of chromosomal imbalance and phenotype in human using ensembl resources
- Wellcome Trust Sanger Institute
- DECIPHER
- More details
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- UNITED KINGDOM
- Greater Manchester
- MANCHESTER
- DMuDB: Diagnostic Mutation Database
- St Mary's Hospital
- National Genetics Reference Laboratory - Manchester
- More details