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Caption : Accreditation =Accreditation
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    • SWITZERLAND
    • Suisse Romande
    • GENÈVE
    • Accreditation
    • Molecular diagnosis of long QT syndrome (KCNQ1, KCNH2, KCNE1, KCNE2, KCNJ2 and SCN5A genes sequencing)
    • Centre Médical Universitaire - CMU
    • More information
    • GERMANY
    • Niedersachsen
    • HANNOVER
    • Accreditation
    • Molecular diagnosis of long QT syndrome (KCNQ1, KCNH2, KCNE1,KCNE2 and SCN5A genes)
    • Medizinische Hochschule Hannover
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • Accreditation
    • Molecular diagnosis of long QT syndrome (KCNQ1, KCNH2, KCNE1,KCNE2 and SCN5A genes)
    • Praxisgemeinschaft für Laboratoriumsmedizin und Humangenetik
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of long QT syndrome type 1, 2, 3, 5 and 6 (KCNE1, KCNE2, KCNH2, KCNQ1, SCN5A genes)
    • Medizinisches Versorgungszentrum Humane Genetik
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular diagnosis of long QT syndrome type 1-3, 5, 6, 8-10 (CACNA1C, CAV3, KCNQ1, KCNE1, KCNE2, KCNH2, SCN5A, SCN4B genes)
    • Bioscientia Institut für Medizinische Diagnostik GmbH
    • More information
    • BELGIUM
    • VLAAMS BRABANT
    • LEUVEN
    • Accreditation
    • Molecular diagnosis of Long QT syndrome (KCNQ1, KCNH2 genes)
    • University Hospitals Leuven - Gasthuisberg
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Accreditation
    • Molecular diagnosis of long QT syndrome (KCNQ1, KCNH2, SCN5A, KCNE1 and KCNE2 genes)
    • Centre Hospitalier Universitaire Vaudois CHUV
    • More information
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • Accreditation
    • Molecular diagnosis of Familial Long QT Syndrome by sequencing of the entire coding region of gene (s) (KCNQ1, KCNH2, SCN5A, KCNE1 & KCNE2 genes)
    • Birmingham Women's NHS Foundation Trust
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Accreditation
    • Molecular diagnosis of long QT syndrome (KCNQ1, KCNH2, KCNE1,KCNE2 and SCN5A genes)
    • Gemeinschaftspraxis Dr. Prager / Dr. Junge / Dr. Hennig / Dr. Linné
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular diagnosis of long QT syndrome type 1-3, 5, 6, 7 and 8 (CACNA1C, KCNE1, KCNE2, KCNH2, KCNJ2, KCNQ1, SCN5A genes)
    • Zentrum für Humangenetik Mannheim
    • More information
    • UNITED KINGDOM
    • Grampian
    • ABERDEEN
    • Accreditation
    • Molecular diagnosis of Long QT syndrome - LQT1, LQT2, LQT3, LQT5, LQT6 (Genes: KCNE1, KCNE2, KCNQ1, KCNH2, SCN5A)
    • Aberdeen Royal Infirmary, Polwarth Building
    • More information
    • UNITED KINGDOM
    • Grampian
    • ABERDEEN
    • Accreditation
    • Molecular diagnosis of Jervell And Lange-Nielsen Syndrome 1 and 2 (Genes: KCNE1, KCNQ1)
    • Aberdeen Royal Infirmary, Polwarth Building
    • More information
    • NETHERLANDS
    • Limburg
    • MAASTRICHT
    • Accreditation
    • Molecular diagnosis of Long QT Syndrome type 2, 3, 5, 6 and 9 (KCNH2, SCN5A, KCNE1, KCNE2 and CAV3 gene)
    • AZM - Academisch Ziekenhuis Maastricht
    • More information
    • NETHERLANDS
    • Limburg
    • MAASTRICHT
    • Accreditation
    • Molecular diagnosis of Jervell and Lange-Nielsen Syndrome type 1 and 2 (KCNQ1 and KCNE1 gene)
    • AZM - Academisch Ziekenhuis Maastricht
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Unexplained Deafness (exome sequencing)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of Conduction Abnormalities (multigene panel; 33 genes)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of Long QT Syndrome type 1, 2, 3, 5, 6 and 9 (KCNQ1, KCNH2, SCN5A, KCNE1, KCNE2 and CAV3 gene)
    • AMC - Academisch Medisch Centrum
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of Jervell and Lange-Nielsen Syndrome (KCNQ1 and KCNE1 gene)
    • AMC - Academisch Medisch Centrum
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of Cardiac Rhythm Disease (multigene panel; 43 genes)
    • AMC - Academisch Medisch Centrum
    • More information
    • UNITED KINGDOM
    • Oxfordshire
    • OXFORD
    • Accreditation
    • Molecular diagnosis of Familial long QT syndrome (KCNQ1, KCNH2, KCNE1, KCNE2, SCN5A genes: mutation screening by sequencing and dosage analysis by MLPA)
    • The Churchill Hospital
    • More information
    • UNITED KINGDOM
    • Oxfordshire
    • OXFORD
    • Accreditation
    • Molecular diagnosis of Jervell and Lange Neilsen syndrome (KCNQ1, KCNE1 gene: mutation screening by sequencing and dosage analysis by MLPA)
    • The Churchill Hospital
    • More information
    • GERMANY
    • Bayern
    • MARTINSRIED
    • Accreditation
    • Molecular diagnosis of long QT syndrome type 1-9 (ANK2, CACNA1C, CAV3, KCNE1, KCNE2, KCNH2, KCNJ2, KCNQ1, SCN4B, SCN5A, SNTA1 genes)
    • Zentrum für Humangenetik und Laboratoriumsmedizin Dr. Klein und Dr. Rost
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of long QT syndrome type 1-13 (ANK2, AKAP9, CACNA1C, CAV3, KCNE1, KCNE2, KCNH2, KCNJ2, KCNQ1, SCN4B, SCN5A, SNTA1 genes)
    • Centogene AG
    • More information
    • GERMANY
    • Baden-Württemberg
    • KARLSRUHE
    • Accreditation
    • Molecular diagnosis of long QT syndrome (KCNQ1, KCNH2, KCNE1,KCNE2 and SCN5A genes)
    • Labor PD Dr. Volkmann und Kollegen
    • More information
    • GERMANY
    • Hessen
    • FRANKFURT AM MAIN
    • Accreditation
    • Molecular diagnosis of long QT syndrome type 1 (KCNQ1, KCNH2 genes)
    • Zentrum für Humangenetik
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of long QT syndrome type 1-12 (ANK2, AKAP9, CACNA1C, CAV3, KCNE1, KCNE2, KCNH2, KCNJ2, KCNQ1, SCN4B, SCN5A, SNTA1 genes)
    • MVZ Fenner & Krasemann
    • More information
    • UNITED KINGDOM
    • County Antrim
    • BELFAST
    • Accreditation
    • Molecular diagnosis of long QT syndrome (KCNQ1, KCNH2, KCNE1, KCNE2, and SCN5A genes sequencing and MLPA)
    • Belfast City Hospital
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • MÜNSTER
    • Accreditation
    • Molecular diagnosis of long QT syndrome type 1-13 (ANK2, AKAP9, CACNA1C, CAV3, KCNE1, KCNE2, KCNH2, KCNJ2, KCNJ5, KCNQ1, SCN4B, SCN5A, SNTA1 genes)
    • Universitätsklinikum Münster
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of long QT syndrome (KCNE1 gene: sequencing)
    • CeGaT GmbH
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • NANTES
    • Molecular diagnosis of long QT syndrome 1, 2, 3, 4, 5, 6 and 7 (KCNQ1, KCNH2, SCN5A, ANK2, KCNE1, KCNE2, KCNJ2 genes)
    • CHU de Nantes - Institut de Biologie
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • NANTES
    • Molecular diagnosis of Jervell-Lange-Nielsen syndrome (KCNQ1 and KCNE1 genes)
    • CHU de Nantes - Institut de Biologie
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of long QT syndrome and Brugada syndrome (KCNQ1, KCNH2 and SCN5A genes)
    • CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Molecular diagnosis of long QT syndrome (KCNQ1, KCNH2, KCNE1, KCNE2, KCNJ2 genes)
    • CHRU de Lille - Centre de biologie pathologie génétique
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Molecular diagnosis of Jervell and Lange-Nielsen syndrome (KCNQ1, KCNE1 genes)
    • Biotecnologie Avanzate Srl
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of familial long QT syndrome (SCN5A gene)
    • IRCCS Ospedale San Raffaele
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of familial long QT syndrome (KCNQ1, KCNE1, KCNE2, KCNH2, ANK2, SCN5A, CACNA1C, CAV3, SCN4B, AKAP9 and SNTA1 genes)
    • Sistemas Genómicos S.L.
    • More information
    • DENMARK
    • Jylland
    • AARHUS
    • Molecular diagnosis of long QT syndrome (SCN5A, KCNE1 and KCNE2 gene sequencing and MLPA)
    • Aarhus Universitetshospital - Skejby
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • SCHLIEREN
    • Molecular diagnosis of Long QT syndrome and Brugada syndrome: complete sequencing of KCNQ1, KCNH2 and SCN5A genes
    • Universität Zürich
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular diagnosis of long QT syndrome (CAV3, KCNE1, KCNE2, KCNH2, KCNJ2, KCNQ1 genes)
    • Praxis Dres. Gencik
    • More information
    • PORTUGAL
    • SUL
    • LISBOA
    • Molecular diagnosis of long QT syndrome type 1, 2, 3 (KCNQ1, KCNH2, HERG, KCNE1 e SCN5A genes): sequencing of the coding region.
    • Faculdade de Medicina da Universidade de Lisboa
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of Long QT syndrome (KCNH2, KCNE1, and KCNE2 genes)
    • Praxis für Humangenetik
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of long QT syndrome type 1, 2 and 4 (KCNQ1, KCNE1, KCNH2 and ANK2 genes: sequencing of the coding region for KCNQ1, KCNH2 and ANK2 genes and sequencing of targeted mutation and delection/duplication analysis by MLPA for KCNE1 gene)
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • REINACH
    • Molecular diagnosis of long QT syndrome type 1, 2, 3, 5 and 6 (KCNQ1, KCNH2, SCN5A, KCNE1 and KCNE2 genes)
    • Diagene Laboratories Inc.
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular diagnosis of familial long QT syndrome (KCNQ1, SCN4B, KCNH2,SCN5A, KCNE1, KCNE2, CAV3, ANK2 genes / entire coding sequence)
    • Centro Inmunológico de Alicante (CIALAB)
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Molecular diagnosis of Inherited Cardiac Arrhythmias - Long QT syndrome types (KCNQ1, KCNH2, SCN5A genes)
    • Universitair Ziekenhuis Brussel - UZBrussel
    • More information
    • HUNGARY
    • Észak-Magyarország
    • BUDAPEST
    • Biochemical genetics diagnosis of familial long QT syndrome by dHPLC analysis
    • Semmelweis University
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • Molecular diagnosis of long QT syndrome type 1 (KCNQ1, KCNH2 genes)
    • Institut für Klinische Genetik Bonn
    • More information
    • SLOVENIA
    • SLOVENIA
    • LJUBLJANA
    • Molecular diagnosis of Long QT syndrome (LQT1 and LQT7 genes)
    • University Medical Centre Ljubljana
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Molecular diagnosis of Long QT syndrome type 3 (SCN5A gene)
    • Diagenom GmbH
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular diagnosis of familial long QT syndrome. KCNQ1 gene.
    • Genetaq
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of familial long QT syndrome (KCNQ1, KCNH2, KCNE1, KCNE2 y KCNJ2 genes - entire coding sequence)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • ROMANIA
    • BUCURESTI
    • BUCURESTI
    • Postnatal molecular diagnosis of familial long QT syndrome (SCN5A, KCNQ1 and KCNH2 genes:deletion/duplication analysis by MLPA; mutation screening and sequencing of the entire coding region)
    • National institute of legal medicine
    • More information
    • SPAIN
    • Galicia
    • A CORUÑA
    • Molecular diagnosis of familial long QT syndrome (SCN5A, CACNA1C, KCNE1, KCNE2, SCN4B, CAV3, KCNH2, KCNQ1 genes)
    • Health In Code
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Molecular diagnosis of long QT syndrome type 1-3, 5, 6, 7 and 8 (KCNE1, KCNE2, KCNH2, KCNJ2, KCNQ1, SCN5A genes: sequencing / MLPA; CACNA1C gene: sequencing)
    • Gemeinschaftspraxis für Humangenetik
    • More information
    • SPAIN
    • Castilla - León
    • SALAMANCA
    • Molecular diagnosis of Romano-Ward and Jervell and Lange-Nielsen syndromes (SCN5A, KCNQ1, KCNH2, KCNE1 genes / HA-CSGE, sequencing)
    • Universidad de Salamanca. Facultad de Medicina
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of long QT syndrome (KCNQ1, KCNH2, SCN5A, KCNE1, KCNE2, CACNA1C and ANK2 genes)
    • IRCCS Ospedale Pediatrico Bambino Gesù
    • More information
    • ITALY
    • LOMBARDIA
    • PAVIA
    • 'Molecular diagnosis of long QT syndrome (KCNQ1, KCNH2, SCN5A, KCNE1, KCNE2 genes; CACNA1C with Timothy syndrome)'
    • Fondazione Salvatore Maugeri
    • More information
    • FRANCE
    • RHONE-ALPES
    • BRON
    • Molecular diagnosis of long QT syndrome and infant death syndrome (KCNQ1, KCNH2, SCN5A, KCNE1 and KCNE2 genes)
    • CHU de Lyon HCL - GH Est
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BAD OEYNHAUSEN
    • Molecular diagnosis of long QT syndrome type 1-13 (ANK2, AKAP9, CACNA1C, CAV3, KCNE1, KCNE2, KCNH2, KCNJ2, KCNJ5, KCNQ1, NOS1AP, SCN4B, SCN5A, SNTA1 genes)
    • Ruhr-Universität Bochum
    • More information
    • DENMARK
    • Sjælland
    • COPENHAGEN
    • Molecular diagnosis of long QT syndrome
    • Statens Serum Institut
    • More information
    • CZECH REPUBLIC
    • South Moravia
    • BRNO
    • Molecular diagnosis of long QT syndrome (KCNQ1, KCNH2 and KCNE1 genes)
    • University hospital Brno
    • More information
    • SPAIN
    • Comunidad Valenciana
    • VALENCIA
    • Molecular diagnosis of Jervell and Lange-Nielsen syndrome (sequencing of KCNE1 and KCNQ1 genes)
    • INCLIVA
    • More information
    • TURKEY
    • TURKEY
    • ISTANBUL
    • Molecular diagnosis of Jervell and Lange-Nielsen syndrome (whole sequence of KVLQT1 and KCNE1 genes)
    • Istanbul University
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of Jervell and Lange-Nielsen syndrome (KCNQ1 and KCNE1 genes: entire coding sequence)
    • Laboratorio de Genética Clínica, S.L.
    • More information
    • SPAIN
    • Andalucía
    • ARMILLA
    • Molecular diagnosis of Jervell and Lange-Nielsen syndrome (entire coding sequence of KCNE1 and KCNQ1 genes)
    • Lorgen G.P.
    • More information
    • SPAIN
    • Madrid
    • MAJADAHONDA
    • Molecular diagnosis of familial long QT syndrome (KCNQ1, KCNH2 and SCN5A genes)
    • Genyca Innova
    • More information
    • FINLAND
    • Finland
    • HELSINKI
    • Molecular diagnosis of Long QT syndrome (AKAP9, ANK2, CACNA1C, CAV3, KCNE1, KCNE2, KCNH2, KCNJ2, KCNJ5, KCNQ1, NOS1AP, SCN4B, SCN5A, SNTA1 genes) Next-generation sequencing
    • Biomedicum Helsinki 2U
    • More information