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Caption : Accreditation =Accreditation
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    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • MARSEILLE
    • Accreditation
    • Molecular diagnosis of early infantile epileptic encephalopathy (STXBP1 and KCNQ2 genes)
    • CHU de Marseille - Hôpital de la Timone
    • More information
    • GERMANY
    • Berlin
    • BERLIN
    • Accreditation
    • Molecular diagnosis of ARX gene-associated diseases (West syndrome, PROUD syndrome, XLAG, MRXARX, PRTS)
    • Charité - Universitätsmedizin Berlin (CVK)
    • More information
    • GERMANY
    • Niedersachsen
    • GÖTTINGEN
    • Accreditation
    • Molecular diagnosis of Ohtahara syndrome (STXBP1 gene)
    • Universitätsmedizin Göttingen
    • More information
    • GERMANY
    • Baden-Württemberg
    • ULM
    • Accreditation
    • Molecular diagnosis of ARX gene-associated diseases (West syndrome, PROUD syndrome, XLAG, MRXARX, PRTS)
    • Universitätsklinikum Ulm
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of mental retardation with epilepsy (ARX, CDKL5 and MECP2 genes)
    • Medizinisch Genetisches Zentrum München
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of Ohtahara syndrome (STXBP1 gene)
    • Medizinisch Genetisches Zentrum München
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of early infantile epileptic encephalopathy 7 and 14 (KCNT1, KCNQ2 genes)
    • Medizinisch Genetisches Zentrum München
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of early infantile epileptic encephalopathy with suppression bursts (SLC25A22 gene: sequencing)
    • Medizinisch Genetisches Zentrum München
    • More information
    • GERMANY
    • Schleswig-Holstein
    • LÜBECK
    • Accreditation
    • Molecular diagnosis of ARX gene-associated diseases (West syndrome, PROUD syndrome, XLAG, MRXARX, PRTS)
    • Universitätsklinikum Schleswig-Holstein - Campus Lübeck
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Accreditation
    • Diagnostic moléculaire des pathologies liées au gène ARX (gène ARX)
    • Centre Hospitalier Universitaire Vaudois CHUV
    • More information
    • DENMARK
    • Sjælland
    • GLOSTRUP
    • Accreditation
    • Prenatal and postnatal molecular diagnosis of ARX-related disorders (mutation screening, carrier analysis)
    • Kennedy Center
    • More information
    • UNITED KINGDOM
    • Lanarkshire
    • GLASGOW
    • Accreditation
    • Molecular diagnosis of Early Infantile Epileptic Encephalopathy by sequencing of the entire coding region of gene (s) (post-natal and pre-natal) (PCDH19 gene)
    • Southern General Hospital
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Accreditation
    • Molecular diagnosis of ARX gene-associated diseases (sequencing / MLPA)
    • Gemeinschaftspraxis Dr. Prager / Dr. Junge / Dr. Hennig / Dr. Linné
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • SCHLIEREN
    • Accreditation
    • Molecular diagnosis of epileptic encephalopathy (entire coding region/ MLPA of ARX, SCN1A, SCN2A, STXBP1, SYNGAP1 genes)
    • Universität Zürich
    • More information
    • UNITED KINGDOM
    • South Glamorgan
    • CARDIFF
    • Accreditation
    • Molecular diagnosis of ARX-associated disorders: West syndrome, X-linked lissencephaly with genital anomalies and mental deficit, Epilepsy and Spascity (ARX gene)
    • University Hospital of Wales
    • More information
    • UNITED KINGDOM
    • South Glamorgan
    • CARDIFF
    • Accreditation
    • Molecular diagnosis of Early Infantile Epileptic Encephalopathy type 4 (EIEE4, STXBP1gene: Molecular diagnosis through sequencing analysis)
    • University Hospital of Wales
    • More information
    • UNITED KINGDOM
    • South Glamorgan
    • CARDIFF
    • Accreditation
    • Molecular diagnosis of Early Infantile Epileptic Encephalopathy type 9 (EIEE9, PCDH19 gene: Molecular diagnosis through sequencing analysis)
    • University Hospital of Wales
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of ARX gene-associated diseases (sequencing / MLPA)
    • GenteQ GmbH
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular diagnosis of early infantile epileptic encephalopathy 2, 3, 7 und 10 (CDKL5, KCNQ2, PNKP, SLC25A22 genes)
    • Zentrum für Humangenetik Mannheim
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular diagnosis of Ohtahara syndrome (STXBP1 gene)
    • Zentrum für Humangenetik Mannheim
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular diagnosis of ARX gene-associated diseases
    • Zentrum für Humangenetik Mannheim
    • More information
    • BELGIUM
    • HAINAUT
    • GOSSELIES
    • Accreditation
    • Molecular diagnosis of ARX-gene related disorders (ARX gene by MLPA and seq)
    • Institut de Pathologie et de Génétique - Gosselies
    • More information
    • GERMANY
    • Bayern
    • REGENSBURG
    • Accreditation
    • Molecular diagnosis of ARX gene-associated diseases (West syndrome, PROUD syndrome, XLAG, MRXARX, PRTS: sequencing, MLPA, NGS panel)
    • Universitätsklinikum Regensburg
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of Early Infantile Epileptic Encephalopathy type 1, 2, 3, 4 and 6 (ARX, CDKL5, SLC25A22, STXBP1 and SCN1A gene)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of Early Infantile Epileptic Encephalopathy type 1, 2, 3, 4, 7, 8, 9, 10, 11 and 12 (ARX, CDKL5, SLC25A22, STXBP1, KCNQ2, ARHGEF9, PCDH19, PNKP, SCN2A and PLCB1 gene)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of Benign Neonatal/Infantile Seizures (multigene panel; 5 genes)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of Epileptic Encephalopathy (multigene panel; 32 genes)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of ARX gene-associated diseases (West syndrome, PROUD syndrome, XLAG, MRXARX, PRTS)
    • Praxis für Humangenetik Freiburg
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of early infantile epileptic encephalopathy (CDKL5, PLCB1 genes)
    • Praxis für Humangenetik Freiburg
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of early infantile epileptic encephalopathy (ARX, CDKL5, KCNQ2, PCDH19, PLCB1, PNKP, SCN1A, SCN2A, SCN8A, SLC25A22, SPTAN1, STXBP1 genes)
    • Centogene AG
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of ARX gene-associated diseases
    • Centogene AG
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • AARGAU
    • Accreditation
    • Molecular diagnosis of ARX gene-associated diseases (ARX gene sequencing and deletion analysis)
    • Kantonsspital Aargau
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of early infantile epileptic encephalopathy (ARX, CDKL5, PLCB1, PNKP, SCN8A, SLC25A18, SLC25A22, STXBP1 genes: sequencing)
    • CeGaT GmbH
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of ARX gene-associated diseases (sequencing)
    • CeGaT GmbH
    • More information
    • FRANCE
    • AQUITAINE
    • BORDEAUX
    • Molecular diagnosis of intellectual deficits linked to an ARX gene mutation
    • CHU de Bordeaux-GH Pellegrin
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of early infantile epileptic encephalopathy (STXBP1 gene)
    • CHU Paris Centre - Hôpital Cochin
    • More information
    • FRANCE
    • RHONE-ALPES
    • LYON
    • Molecular diagnosis of early infantile epileptic encephalopathy (STXBP1 gene)
    • CHU de Lyon HCL - GH Edouard Herriot
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of early infantile epileptic encephalopathy (KCNQ2, STXBP1 genes)
    • CHU Paris - Hôpital Necker-Enfants Malades
    • More information
    • ITALY
    • VENETO
    • COSTOZZA DI LONGARE
    • Molecular diagnosis of rare intellectual deficit associated to ARX (ARX gene)
    • B.I.R.D. Foundation
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Molecular diagnosis of early infantile epileptic encephalopathy 10 (PNKP gene)
    • Universitätsklinikum Freiburg
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of early infantile epileptic encephalopathy (SCN8A gene)
    • Sistemas Genómicos S.L.
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular diagnosis of ARX gene-associated diseases (West syndrome, PROUD syndrome, XLAG, MRXARX, PRTS)
    • Praxis Dres. Gencik
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular diagnosis of early infantile epileptic encephalopathy (ARX, CDKL5, KCNQ2, KCNT1, PCDH19, SCN1A, SCN2A, SPTAN1 genes)
    • Praxis Dres. Gencik
    • More information
    • GERMANY
    • Baden-Württemberg
    • STUTTGART
    • Molecular diagnosis of mental retardation with epilepsy (ARX, CDKL5 and MECP2 genes)
    • Klinikum Stuttgart - Standort Olgahospital
    • More information
    • FRANCE
    • CENTRE
    • TOURS
    • Molecular diagnosis of ARX-related epileptic encephalopathy (ARX gene mutations)
    • CHRU de Tours - Hôpital Bretonneau
    • More information
    • BELGIUM
    • ANTWERPEN
    • ANTWERPEN
    • Molecular diagnosis of Early infantile epileptic encephalopathy (KCNQ2, STXBP1 genes)
    • University of Antwerp - UA
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Early infantile epileptic encephalopathy (STXBP1, SCN8A, PCDH19 and CDKL5 genes: sequencing of the entire coding region)
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular diagnosis of early infantile epileptic encephalopathy (ARX gene / sequencing)
    • Centro Inmunológico de Alicante (CIALAB)
    • More information
    • POLAND
    • Poznan
    • POZNAN
    • Molecular diagnosis of ARX-related mental retardation (ARX gene: dup24 mutation)
    • NZOZ Centrum Genetyki Medycznej Genesis
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of early infantile epileptic encephalopathy (STXBP1 gene - entire coding sequence)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Molecular diagnosis of mental retardation with epilepsy (ARX, CDKL5 and MECP2 genes: sequencing, MLPA)
    • Gemeinschaftspraxis für Humangenetik
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Molecular diagnosis of ARX gene-associated diseases (sequencing / MLPA)
    • Gemeinschaftspraxis für Humangenetik
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular diagnosis of ARX gene mutations
    • Policlinico Universitario "A. Gemelli"
    • More information
    • GERMANY
    • Bayern
    • REGENSBURG
    • Molecular diagnosis of ARX gene-associated diseases (West syndrome, PROUD syndrome, XLAG, MRXARX, PRTS)
    • Universität Regensburg
    • More information
    • DENMARK
    • Fyn
    • ODENSE
    • Molecular diagnosis of ARX-related diseases (gene sequencing)
    • Amplexa Genetics A/S
    • More information
    • ISRAEL
    • ISRAEL
    • HOLON
    • Molecular diagnosis of ARX-related disorders (ARX, sequencing analysis, PGD)
    • Wolfson Medical Center
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of early infantile epileptic encephalopathy (entire coding sequence of ARX, SLC25A22 and STXBP1 genes)
    • Laboratorio de Genética Clínica, S.L.
    • More information