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Caption : Accreditation =Accreditation
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    • GERMANY
    • Nordrhein-Westfalen
    • DÜSSELDORF
    • Accreditation
    • Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
    • Heinrich-Heine-Universität Düsseldorf
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
    • Medizinisch Genetisches Zentrum München
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
    • Bioscientia Institut für Medizinische Diagnostik GmbH
    • More information
    • UNITED KINGDOM
    • Greater Manchester
    • MANCHESTER
    • Accreditation
    • Molecular diagnosis of Steroid-Resistant Nephrotic Syndrome - SRNS (NPHS2 gene: bi-directional fluorescent sequencing of the whole coding sequence)
    • St Mary's Hospital
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Accreditation
    • Molecular diagnosis of Familial Mesangial Sclerosis (WT1 gene)
    • Institut de Pathologie et de Génétique - Gosselies
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of Nephrotic Syndrome type 3 (PLCE1 gene)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of Nephrotic Syndrome with Diffuse Mesangial Sclerosis (WT1 gene)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of Nephrotic Syndrome type 2, 3 and 4 (NPHS2, PLCE1 and WT1 gene)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • GERMANY
    • Hessen
    • FRANKFURT AM MAIN
    • Accreditation
    • Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
    • Zentrum für Humangenetik
    • More information
    • GERMANY
    • Berlin
    • BERLIN
    • Accreditation
    • Molecular diagnosis of nephrotic syndrome (ACTN4, INF2, NPHS1, NPHS2, PLCE1, TRPC6, WT1 gene)
    • IFLb Laboratoriumsmedizin Berlin GmbH
    • More information
    • FRANCE
    • 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
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of idiopathic nephrotic syndrome, steroid-resistant (NPHS2 gene)
    • Laboratorio Genoma
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • Molecular diagnosis of idiopathic nephrotic syndrome (ACTN4, ARHGDIA, INF2, NPHS1, NPHS2, PLCE1, PTPRO, TRPC6 genes)
    • Universitätsklinikum Köln
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
    • Universitätsklinikum Köln
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Molecular diagnosis of mesangial sclerosis diffuse . WT1 gene
    • Fundació Puigvert
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Molecular diagnosis of nephrotic syndrome, idiopathic, steroid-resistant. WT1, NPHS2 genes
    • Fundació Puigvert
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
    • Praxis Dres. Gencik
    • More information
    • GERMANY
    • Sachsen
    • WEIßWASSER
    • Molecular diagnosis of nephrotic syndrome with diffuse mesangial sclerosis (WT1, PLCE1 genes)
    • Praxis Dr. Mato Nagel
    • More information
    • GERMANY
    • Sachsen
    • WEIßWASSER
    • Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
    • Praxis Dr. Mato Nagel
    • More information
    • PORTUGAL
    • SUL
    • LISBOA
    • Molecular diagnosis of congenital and steroid-resistant nephrotic syndrome (NPHS1 and NPHS2 genes)
    • Faculdade de Medicina da Universidade de Lisboa
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Familial idiopathic steroid-resistant nephrotic syndrome (PLCE1 gene): Sequencing of the entire coding region
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of congenital and steroid-resistant nephrotic syndrome (NPHS2 gene): Sequencing of the entire coding region
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular diagnosis of familial idiopathic steroid-resistant nephrotic syndrome (NPHS1, NPHS2, WT1 genes / entire coding sequence)
    • Centro Inmunológico de Alicante (CIALAB)
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • MÜNSTER
    • Molecular diagnosis of nephrotic syndrome (ACTN4, NPHS1, NPHS2, TRPC6, WT1 genes)
    • Universitätsklinikum Münster
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • MÜNSTER
    • Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
    • Universitätsklinikum Münster
    • More information
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • Molecular diagnosis of diffuse mesangial sclerosis (WT1 gene)
    • Karolinska University Hospital - Solna
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Molecular diagnosis of nephrotic syndromes (NPHS1, NPHS2, WT1, PLCE and ACTN4 genes)
    • "Aghia Sophia" Children's Hospital
    • More information
    • SPAIN
    • Comunidad Valenciana
    • VALENCIA
    • Molecular diagnosis of mesangial sclerosis diffuse. WT1 gene
    • Progerie Molecular, S.L.
    • More information
    • GERMANY
    • 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.
    • More information
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
    • Universitätsklinikum Heidelberg
    • More information
    • SPAIN
    • 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.
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis (entire coding sequence of PLCE1, WT1 and PTPRO genes)
    • Laboratorio de Genética Clínica, S.L.
    • More information
    • SPAIN
    • Andalucía
    • ARMILLA
    • Molecular diagnosis of familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis (entire coding sequence of WT1, NPHS1 and NPHS2 genes)
    • Lorgen G.P.
    • More information
    • SPAIN
    • Andalucía
    • ARMILLA
    • Molecular diagnosis of familial and sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis (entire coding sequence of WT1 gene)
    • Lorgen G.P.
    • More information
    • GERMANY
    • Berlin
    • BERLIN
    • Molecular diagnosis of nephrotic syndrome (ACTN4, INF2, NPHS1, NPHS2, PLCE1, TRPC6, WT1 genes: sequencing)
    • ATG GenMed GmbH
    • More information
    • FINLAND
    • Finland
    • HELSINKI
    • Molecular diagnosis of nehprotic syndrome (ACTN4, CD2AP, INF2, LAMB2, NPHS1, NPHS2, PLCE1, TRPC6, WT1 genes) Next-generation sequencing
    • Biomedicum Helsinki 2U
    • More information