Skip to
Languages :
Français
English
Español
Deutsch
Italiano
Orphanet index
The portal for rare diseases and orphan drugs
Homepage
Help
Contact us
Main menu :
Rare diseases
Orphan drugs
Clinics
Diagnostic tests
Research and trials
Patient organisations
Directory of resources
Other information
Submenu :
Research projects
Clinical trials
Licencing offers
Registries & biobanks
Technology & Know-How
Register / Update your activity
Navigation tree :
Homepage
Research and trials
Research projects
Print
Search by disease/gene
Search by disease/gene
MISSING CONTENT
*
(*) mandatory field
Disease name
Gene name or symbol
All countries
Austria
Belgium
Bulgaria
Cyprus
Czech republic
Denmark
Estonia
Finland
France
Germany
Greece
Hungary
Ireland
Israel
Italy
Lebanon
Morocco
Netherlands
Poland
Portugal
Romania
Spain
Sweden
Switzerland
Turkey
United kingdom
Country
Search by disease/gene
Other search option(s)
Search by research category
Search by institution/laboratory
Search by professional
Search by sponsor/funding body
Search by partnership category
3 Result(s)
Partnership : Academics =
, Industrials =
, Financial investitors =
BELGIUM
ARRONDISSEMENT BRUSSEL HOOFDSTAD
BRUXELLES
Natural course and phenotype in patients with familial juvenile hyperuricemic nephropathy and harbouring UMOD mutations
Université Catholique de Louvain - UCL
Centre de Génétique Humaine de l'UCL
More details
FRANCE
PROVENCE-ALPES-COTE D'AZUR
MARSEILLE
TSHIRTS & SOXs: Teashirt and Sox genes in the congenital kidney anomalies
Parc scientifique de Luminy
Institut de Biologie du Développement de Marseille-Luminy
More details
POLAND
Poznan
POZNAN
Etiological analysis of congenital malformations of urinary system in children
Uniwersytet Medyczny w Poznaniu - Poznan University of Medical Sciences
Katedra i Zaklad Gentyki Medycznej (Department of Medical Genetics)
More details
Orphanet
Footer:
Copyright
Languages :
Français
English
Español
Deutsch
Italiano