Didascalia
: Accreditato
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- GERMANIA
- Nordrhein-Westfalen
- DÜSSELDORF
- Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
- Heinrich-Heine Universität Düsseldorf
- Ulteriori informazioni
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- Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
- Medizinisch Genetisches Zentrum München
- Ulteriori informazioni
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- GERMANIA
- Rheinland-Pfalz
- INGELHEIM AM RHEIN
- Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
- Bioscientia Institut für Medizinische Diagnostik GmbH
- Ulteriori informazioni
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- Molecular diagnosis of Nephrotic Syndrome Type 2 (sporadic, idiopathic) (NPHS2, WT1 genes)
- Institut de Pathologie et de Génétique - Gosselies
- Ulteriori informazioni
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- PAESI BASSI
- Gelderland
- NIJMEGEN
- Molecular diagnosis of Nephrotic Syndrome with Diffuse Mesangial Sclerosis (WT1 gene)
- UMC St Radboud - Universitair Medisch Centrum St Radboud
- Ulteriori informazioni
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- GERMANIA
- Hessen
- FRANKFURT AM MAIN
- Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
- Zentrum für Humangenetik
- Ulteriori informazioni
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- FRANCIA
- ILE-DE-FRANCE
- PARIS
- Molecular diagnosis of nephrotic syndrome familial or sporadic steroid-resistant (PLCE1 and WT1 gene mutations)
- CHU Paris - Hôpital Necker - Enfants Malades
- Ulteriori informazioni
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- FRANCIA
- HAUTE-NORMANDIE
- ROUEN
- Molecular cytogenetic diagnosis of WT1 gene deletion -associated diseases
- CHU de Rouen - Hôpital Charles Nicolle
- Ulteriori informazioni
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- GERMANIA
- Nordrhein-Westfalen
- KÖLN
- Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
- Klinikum der Universität zu Köln
- Ulteriori informazioni
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- SPAGNA
- Cataluña
- BARCELONA
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- SPAGNA
- Cataluña
- BARCELONA
- Molecular diagnosis of nephrotic syndrome, idiopathic, steroid-resistant. WT1, NPHS2 genes
- Fundació Puigvert
- Ulteriori informazioni
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- GERMANIA
- Niedersachsen
- OSNABRÜCK
- Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
- Praxis Dres. Gencik
- Ulteriori informazioni
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- GERMANIA
- Sachsen
- WEIßWASSER
- Molecular diagnosis of nephrotic syndrome with diffuse mesangial sclerosis (WT1, PLCE1 genes)
- Praxis Dr. Mato Nagel
- Ulteriori informazioni
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- GERMANIA
- Sachsen
- WEIßWASSER
- Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
- Praxis Dr. Mato Nagel
- Ulteriori informazioni
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- GERMANIA
- Nordrhein-Westfalen
- MÜNSTER
- Molecular diagnosis of nephrotic syndrome (ACTN4, NPHS1, NPHS2, TRPC6, WT1 genes)
- Universitätsklinikum Münster
- Ulteriori informazioni
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- GERMANIA
- Nordrhein-Westfalen
- MÜNSTER
- Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
- Universitätsklinikum Münster
- Ulteriori informazioni
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- SVEZIA
- Stockholms läns landsting
- STOCKHOLM
- Molecular diagnosis of diffuse mesangial sclerosis (WT1 gene)
- Karolinska University Hospital - Solna
- Ulteriori informazioni
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- Molecular diagnosis of nephrotic syndromes (NPHS1, NPHS2, WT1, PLCE and ACTN4 genes)
- "Aghia Sophia" Children's Hospital
- Ulteriori informazioni
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- SPAGNA
- Comunidad Valenciana
- VALENCIA
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- GERMANIA
- Nordrhein-Westfalen
- MÜNSTER
- Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
- KfH Kuratorium für Dialyse und Nierentransplantation e.V.
- Ulteriori informazioni
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- GERMANIA
- Baden-Württemberg
- HEIDELBERG
- Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
- Universitätsklinikum Heidelberg
- Ulteriori informazioni
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- SPAGNA
- Madrid
- SAN SEBASTIÁN DE LOS REYES
- Molecular diagnosis of idiopathic steroid-resistant nephrotic syndrome, familial and sporadic (entire coding sequence of NPHS1, NPHS2 and WT1 genes)
- LABORATORIO DE GENÉTICA CLÍNICA S.L.
- Ulteriori informazioni
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- Molecular diagnosis of familial and sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis (entire coding sequence of WT1 gene)
- LORGEN G.P.
- Ulteriori informazioni
