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Caption : Accreditation =Accreditation
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    • FRANCE
    • MIDI-PYRENEES
    • TOULOUSE
    • Accreditation
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • CHU de Toulouse - Hôpital Purpan
    • More information
    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • MARSEILLE
    • Accreditation
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • CHU de Marseille - Hôpital de la Timone
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • DORTMUND
    • Accreditation
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
    • More information
    • GERMANY
    • Niedersachsen
    • HANNOVER
    • Accreditation
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Medizinische Hochschule Hannover
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • Accreditation
    • Molecular diagnosis of Pendred syndrome
    • Praxisgemeinschaft für Laboratoriumsmedizin und Humangenetik
    • More information
    • GERMANY
    • Bayern
    • NEU-ULM
    • Accreditation
    • Molecular diagnosis of Pendred syndrome
    • Paxis und Labor Dr. med Karl Mehnert
    • More information
    • GERMANY
    • Baden-Württemberg
    • ULM
    • Accreditation
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Universitätsklinikum Ulm
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular diagnosis of Pendred syndrome (FOXI1, SLC26A4 genes: sequencing)
    • Bioscientia Institut für Medizinische Diagnostik GmbH
    • More information
    • BELGIUM
    • ANTWERPEN
    • ANTWERPEN-EDEGEM
    • Accreditation
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • University and University Hospital of Antwerp - UZA
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • Accreditation
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Erasme Hospital - ULB
    • More information
    • GERMANY
    • Bayern
    • WÜRZBURG
    • Accreditation
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Universität Würzburg - Biozentrum
    • More information
    • UNITED KINGDOM
    • Tayside
    • DUNDEE
    • Accreditation
    • Molecular diagnosis of Pendred syndrome (by sequence analysis of SLC26A4 and FOXI1 genes and deletion testing by MLPA of SLC26A4)
    • Ninewells Hospital
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Great Ormond Street Hospital NHS Trust
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene: sequencing / MLPA)
    • GenteQ GmbH
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of Pendred Syndrome (SLC26A4 gene)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Unexplained Deafness (exome sequencing)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of Pendred Syndrome (SLC26A4 gene)
    • AMC - Academisch Medisch Centrum
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Praxis für Humangenetik Freiburg
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Centogene AG
    • More information
    • BELGIUM
    • ANTWERPEN
    • ANTWERPEN
    • Accreditation
    • Neonatal screening: Biochemical diagnosis of Congenital Hypothyroidism (TSH: GSP (Delfia method), bloodspots)
    • Provinciaal Centrum voor opsporing van Metabole Aandoeningen (PCMA) - Antwerpen
    • More information
    • GERMANY
    • Hessen
    • FRANKFURT AM MAIN
    • Accreditation
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Zentrum für Humangenetik
    • More information
    • SWEDEN
    • Västra Götalandsregionen
    • GÖTEBORG
    • Accreditation
    • Molecular diagnosis of Pendred syndrome (SLC26A4 and FOXI1 genes)
    • Sahlgrenska University Hospital
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • AARGAU
    • Accreditation
    • Molecular diagnosis of Pendred syndrome (SLC6A4 gene sequencing and deletion analysis)
    • Kantonsspital Aargau
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Accreditation
    • Newborn screening : Biochemical diagnosis of congenital hypothyroidism (TSH)
    • Universitätsklinikum Carl Gustav Carus an der TU Dresden
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene: sequencing)
    • CeGaT GmbH
    • More information
    • FRANCE
    • RHONE-ALPES
    • GRENOBLE
    • Neonatal screening of hypothyroidism
    • CHU de Grenoble site Nord - Institut de biologie et de pathologie
    • More information
    • FRANCE
    • RHONE-ALPES
    • BRON
    • Neonatal screening of congenital hypothyroidism
    • CHU de Lyon-GH Est - Hospices Civils de Lyon
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of Pendred syndrome (SLC26A4 complete gene and promoter sequencing)
    • CHU Paris - Hôpital Necker-Enfants Malades
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Neonatal screening of congenital hypothyroidism
    • CHRU de Lille - Centre de biologie pathologie génétique
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • CHRU de Lille - Centre de biologie pathologie génétique
    • More information
    • FRANCE
    • BASSE-NORMANDIE
    • CAEN
    • Neonatal screening of hypothyroidism
    • CHU de Caen - Hôpital de la Côte de Nacre
    • More information
    • ITALY
    • LIGURIA
    • GENOVA
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Ospedali Galliera
    • More information
    • ITALY
    • VENETO
    • COSTOZZA DI LONGARE
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • B.I.R.D. Foundation
    • More information
    • ITALY
    • CAMPANIA
    • NAPOLI
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Biotecnologie Avanzate Srl
    • More information
    • ITALY
    • PUGLIA
    • SAN GIOVANNI ROTONDO
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • IRCCS Ospedale Casa Sollievo della Sofferenza - Polamb. Giovanni Paolo II
    • More information
    • GERMANY
    • Schleswig-Holstein
    • KIEL
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Universitätsklinikum Schleswig-Holstein - Campus Kiel
    • More information
    • ITALY
    • VENETO
    • PADOVA
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Azienda Ospedaliera Universitaria di Padova
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • FERRARA
    • Molecular diagnosis of Pendred/EVA syndrome (SLC26A4 gene)
    • Azienda Ospedaliero-Universitaria di Ferrara
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Universitätsklinikum Köln
    • More information
    • SPAIN
    • Galicia
    • SANTIAGO DE COMPOSTELA
    • Biochemical diagnosis of congenital hypothyroidism
    • CHUS - Complejo Hospitalario Universitario de Santiago
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Sistemas Genómicos S.L.
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Immunological diagnosis of congenital hypothyroidism
    • Tartu University Hospital
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Praxis für Humangenetik
    • More information
    • BELGIUM
    • LIEGE
    • LIEGE
    • Neonatal screening: Biochemical diagnosis of Congenital Hypothyroidism (TSH: ELISA, bloodspots)
    • CHU Sart Tilman - Liège
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene): sequencing and deletion/duplication analysis by MLPA
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene / entire coding sequence)
    • Centro Inmunológico de Alicante (CIALAB)
    • More information
    • SPAIN
    • Murcia
    • EL PALMAR
    • Biochemical diagnosis of Hypothyroidism congenital
    • Hospital Universitario Virgen de la Arrixaca
    • More information
    • NORWAY
    • Nord-Norge
    • TROMSØ
    • Molecular diagnosis of Pendred syndrome
    • UNN - Universitetssykehuset Nord-Norge - University hospital of North Norway
    • More information
    • ITALY
    • CALABRIA
    • CATANZARO
    • Biochemical diagnosis of congenital hypothyroidism
    • Azienda Ospedaliera "Mater Domini"
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Institut für Klinische Genetik Bonn
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • MAINZ
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Universitätsmedizin Mainz
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Genetaq
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • GERMANY
    • Baden-Württemberg
    • ULM
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • MVZ Humangenetik Ulm
    • More information
    • SPAIN
    • Castilla - León
    • SALAMANCA
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene / sequencing)
    • Universidad de Salamanca. Facultad de Medicina
    • More information
    • FRANCE
    • ALSACE
    • STRASBOURG
    • Neonatal screening of hypothyroidism
    • CHU de Strasbourg - Hôpital Civil
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • ANGERS
    • FRANCE
    • PAYS DE LA LOIRE
    • NANTES
    • Neonatal screening of hypothyroidism
    • CHU de Nantes - Hôpital Mère-Enfant
    • More information
    • FRANCE
    • BOURGOGNE
    • DIJON
    • Neonatal screening of hypothyroidism
    • CHU de Dijon - Plateau technique de Biologie
    • More information
    • FRANCE
    • AQUITAINE
    • PESSAC
    • Neonatal screening of hypothyroidism
    • CHU de Bordeaux-GH Sud - Hôpital Haut-Lévêque
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Neonatal screening of hypothyroidism
    • Centre régional de dépistage néonatal
    • More information
    • FRANCE
    • FRANCHE-COMTE
    • BESANÇON
    • Neonatal screening of hypothyroidism
    • CHRU de Besançon - Hôpital Saint-Jacques
    • More information
    • ITALY
    • LIGURIA
    • GENOVA
    • Biochemical neonatal screening of congenital hypothyroidism
    • IRCCS Istituto G. Gaslini - Ospedale Pediatrico
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of congenital hypothyroidism (TTF1 gene)
    • IRCCS Ospedale Pediatrico Bambino Gesù
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of congenital hypothyroidism
    • Croce Rossa Italiana
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Biochemical and molecular diagnosis of congenital hypothyroidism (DUOX2, DUOXA2 genes)
    • Hospital Clínic de Barcelona
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Biochemical diagnosis of hypothyroidism, congenital
    • Institut de Recerca Hospital Universitari Vall d'Hebron
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of Pendred syndrome. SLC26A4 gene.
    • Hospital Universitario Ramón y Cajal
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of congenital hypothyroidism (DUOX2, DUOXA2, FOXE1, FOXI1, PAX8, SECISBP2, SLC16A2, SLC5A5, TG, THRB, TPO, TRH, TRHR, TSHB, TSHR genes)
    • Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
    • More information
    • SPAIN
    • Galicia
    • SANTIAGO DE COMPOSTELA
    • Molecular diagnosis of lipodistrophies and Pendred syndrome
    • Universidad de Santiago de Compostela. Facultad de Medicina
    • More information
    • ROMANIA
    • CLUJ
    • CLUJ
    • Biochemical diagnosis of congenital hypothyroidism
    • Spitalul de Pediatrie Copii Cluj
    • More information
    • CYPRUS
    • Cyprus
    • LIMASSOL
    • Neonatal screening of congenital hypothyroidism
    • Centre for preventive paediatrics
    • More information
    • CZECH REPUBLIC
    • Capital City Prague
    • PRAHA
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene)
    • Motol university hospital - 2nd Medical School Charles University Prague
    • More information
    • LITHUANIA
    • DZUKIJA
    • VILNIUS
    • Biochemical neonatal screening of congenital hypothyroidism
    • Vilnius University Hospital Santariskiu Klinikos
    • More information
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Newborn screening : Biochemical diagnosis of congenital hypothyroidism
    • Universitätsklinikum Heidelberg
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Biochemical diagnosis of congenital hypothyroidism
    • Ospedale dei Bambini ''Vittore Buzzi"
    • More information
    • ITALY
    • PIEMONTE
    • TORINO
    • Biochemical diagnosis of congenital hypothyroidism
    • A.O. Città della Salute e della Scienza di Torino - Ospedale Regina Margherita
    • More information
    • NETHERLANDS
    • Zuid-Holland
    • CAPELLE AAN DEN IJSSEL
    • Immunochemical diagnosis of congenital hypothyroidism (TSH, TBG)
    • IJsselland Ziekenhuis
    • More information
    • NETHERLANDS
    • Utrecht
    • BILTHOVEN
    • Newborn screening: Biochemical diagnosis of Congenital Hypothyroidism (Analyte: Thyroxine, Thyroid-Stimulating Hormone and Thyroxine-Binding Globulin)
    • RIVM - Rijksinstituut voor Volksgezondheid en Milieu
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of Pendred syndrome (entire coding sequence of SLC26A4 gene)
    • Laboratorio de Genética Clínica, S.L.
    • More information
    • SPAIN
    • Andalucía
    • CAMPANILLAS
    • Molecular diagnosis of Pendred syndrome (SLC26A4 gene / sequencing)
    • GenoClinics
    • More information
    • SLOVAKIA
    • Bratislavsky kraj
    • BRATISLAVA
    • PENDRED syndrome (gene SLC26A4 - direct sequencing)
    • Slovak Academy of Sciences
    • More information