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Caption : Accreditation =Accreditation
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    • GERMANY
    • Nordrhein-Westfalen
    • DÜSSELDORF
    • Accreditation
    • Molecular diagnosis of congenital nephrotic syndrome, finnish type (NPHS1 gene)
    • Heinrich-Heine-Universität Düsseldorf
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular diagnosis of congenital nephrotic syndrome, finnish type (NPHS1 gene)
    • Bioscientia Institut für Medizinische Diagnostik GmbH
    • More information
    • FINLAND
    • Finland
    • HELSINKI
    • Accreditation
    • Molecular diagnosis of Finnish type congenital nephrotic syndrome (NPHS1 gene c.121_122del and c.3325C>T)
    • HUCH - Helsinki University Central Hospital
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Accreditation
    • Molecular diagnosis of Nephrotic Syndrome Type 1 (congenital Finnish) (NPHS1 gene)
    • Institut de Pathologie et de Génétique - Gosselies
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of Congenital Nephrotic Syndrome, Finnish type (NPHS1 gene)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of Congenital Nephrotic Syndrome, Finnish type (NPHS1 gene)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of nephrotic syndrome (NPHS1, NPHS2 genes)
    • Praxis für Humangenetik Freiburg
    • More information
    • GERMANY
    • Bayern
    • MARTINSRIED
    • Accreditation
    • Molecular diagnosis of nephrotic syndrome (ACTN4, CD2AP, COQ6, INF2, LAMB2, NPS1, NPHS2, PLCE1, TRPC6, WT1 genes)
    • Zentrum für Humangenetik und Laboratoriumsmedizin Dr. Klein und Dr. Rost
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of congenital nephrotic syndrome, finnish type (NPHS1 gene)
    • Centogene AG
    • More information
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Accreditation
    • Molecular diagnosis of congenital nephrotic syndrome, finnish type (NPHS1 gene)
    • Universitätsklinikum Heidelberg
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Accreditation
    • Preimplantation genetic diagnosis of congenital nephrotic syndrome, Finnish type (NPHS1 gene)
    • Sistemas Genómicos S.L.
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of nephrotic syndromes (NPHS1 gene mutations)
    • CHU Paris - Hôpital Necker-Enfants Malades
    • More information
    • FRANCE
    • ALSACE
    • SCHILTIGHEIM
    • Preimplantation genetic diagnosis of congenital nephrotic syndrome, Finnish type (NPHS1 gene)
    • Centre Médico-Chirurgical et Obstétrical (CMCO)
    • 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
    • SPAIN
    • Cataluña
    • BARCELONA
    • Molecular diagnosis of nephrotic syndrome congenital Finnish type. NPHS1 gene
    • Fundació Puigvert
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of congenital nephrotic syndrome, Finnish type (NPHS1 gene)
    • Sistemas Genómicos S.L.
    • More information
    • GERMANY
    • Sachsen
    • WEIßWASSER
    • Molecular diagnosis of congenital nephrotic syndrome, finnish type (NPHS1 gene)
    • 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
    • GERMANY
    • Nordrhein-Westfalen
    • MÜNSTER
    • Molecular diagnosis of congenital nephrotic syndrome, finnish type (NPHS1 gene)
    • Universitätsklinikum Münster
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Molecular diagnosis of congenital nephrotic syndrome, finnish type (NPHS1 gene)
    • Diagenom GmbH
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular diagnosis of congenital nephrotic syndrome of the Finnish type. NPHS1 gene.
    • Genetaq
    • More information
    • SPAIN
    • Castilla - León
    • SALAMANCA
    • Molecular diagnosis of nephrotic syndrome (NPHS1 gene / sequencing)
    • Universidad de Salamanca. Facultad de Medicina
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Biochemical diagnosis of congenital nephrotic syndrome, finnish type
    • CHU Paris - Hôpital Robert Debré
    • More information
    • ITALY
    • SICILIA
    • MESSINA
    • Molecular diagnosis of congenital nephrotic syndrome, Finnish type (NPHS1 gene)
    • A.O.U. Policlinico "G. Martino"
    • More information
    • FINLAND
    • Finland
    • OULU
    • Molecular diagnosis of congenital nephrotic syndrome, finnish type (NPHS1 gene)
    • Oulu University Hospital
    • More information
    • FINLAND
    • Finland
    • TURKU
    • Molecular diagnosis of congenital nephrotic syndrome, finnish type (NPHS1 gene)
    • Turku University Hospital
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Molecular diagnosis of nephrotic syndromes (NPHS1, NPHS2, WT1, PLCE and ACTN4 genes)
    • "Aghia Sophia" Children's Hospital
    • More information
    • LEBANON
    • Beyrouth
    • BEIRUT
    • Molecular diagnosis of congenital nephrotic syndrome finnish type (complete NPHS1 gene sequencing)
    • Université Saint-Joseph
    • More information
    • ITALY
    • PUGLIA
    • FOGGIA
    • Molecular diagnosis of congenital nephrotic syndrome, Finnish type (NPHS1, NPHS2, WT1, CD2AP, TRCP6 genes)
    • Azienda Ospedaliero-Universitaria Ospedali Riuniti
    • More information
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Molecular diagnosis of congenital nephrotic syndrome, finnish type (NPHS1 gene)
    • Universitätsklinikum Heidelberg
    • 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