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12 Risultato/i
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- Austrian Country Node of the Human Variome Project (HVP)
- Medizinische Universität Innsbruck
- Sektion Humangenetik
- Ulteriori dettagli
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- BELGIO
- ARRONDISSEMENT BRUSSELS-CAPITAL
- BRUSSELS
- EUNEFRON: registry of the European network for the study of orphan nephropathies
- Cliniques Universitaires UCL de Saint Luc - UCLStLuc
- Laboratory of Nephrology
- Ulteriori dettagli
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- DANIMARCA
- Sjælland
- COPENHAGEN
- Mendelian cytogenetics network online database
- The Panum Institute-University of Copenhagen
- Department of Cellular and Molecular Medicine
- Ulteriori dettagli
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- Biobank of the Estonian genome center
- Tartu University Hospital
- Centre of Genetics - United laboratories
- Ulteriori dettagli
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- FRANCIA
- 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
- Ulteriori dettagli
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- GERMANIA
- Niedersachsen
- GÖTTINGEN
- European Alport therapy registry
- Universitätsmedizin Göttingen
- Abteilung Nephrologie und Rheumatologie
- Ulteriori dettagli
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- MoHuMuDa : Moroccan Human Mutation Database
- Institut National d'Hygiène
- Département de génétique médicale
- Ulteriori dettagli
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- PAESI BASSI
- Noord-Holland
- AMSTERDAM
- ESPN/ERA-EDTA Registry: European Registry for Children on Renal Replacement Therapy
- AMC - Academisch Medisch Centrum
- Afdeling Klinische Informatiekunde
- Ulteriori dettagli
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- REGNO UNITO; GRAN BRETAGNA
- Avon
- BRISTOL
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- REGNO UNITO; GRAN BRETAGNA
- Avon
- BRISTOL
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- REGNO UNITO; GRAN BRETAGNA
- Greater Manchester
- MANCHESTER
- DMuDB: Diagnostic Mutation Database
- St Mary's Hospital
- National Genetics Reference Laboratory - Manchester
- Ulteriori dettagli
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- SPAGNA
- Cataluña
- BARCELONA
- Spanish registry of renal hereditary diseases
- Fundació Puigvert
- Servicio de Nefrología
- Ulteriori dettagli