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Caption : Accreditation =Accreditation ;

    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of generalized epilepsy with febrile seizures plus (GABRD, GABRG2, SCN1A, SCN1B, SCN2A genes)
    • Medizinisch Genetisches Zentrum München
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Accreditation
    • Molecular diagnosis of generalized epilepsy with febrile seizures plus (GABRD, GABRG2, SCN1A, SCN1B, SCN2A genes: sequencing, MLPA)
    • Medizinische Genetik Dresden
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular diagnosis of Dravet syndrome / GEFS+ (SCN1A, SCN2A, SCN1B, SCN9A genes)
    • Zentrum für Humangenetik Mannheim
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular diagnosis of benign infantile seizures (SCN2A gene)
    • Zentrum für Humangenetik Mannheim
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of Generalized Epilepsy with Febrile Seizures plus (GABRG2, SCN1A, SCN1B and SCN2A gene)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of Benign Familial Neonatal-Infantile Seizures (SCN2A gene)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of generalized epilepsy with febrile seizures plus (GABRD, GABRG2, SCN1A, SCN1B, SCN2A genes)
    • Praxis für Humangenetik Freiburg
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of benign infantile seizures (SCN2A gene)
    • 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)
    • Institute of Molecular Diagnostics
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of generalized epilepsy with febrile seizures plus (GABRD, GABRG2, SCN1A, SCN1B, SCN2A, SCN9A genes)
    • Institute of Molecular Diagnostics
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of benign familial neonatal-infantile seizures (SCN2A gene)
    • Institute of Molecular Diagnostics
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of generalized epilepsy with febrile seizures plus (GABRD, GABRG2, SCN1A, SCN1B, SCN2A genes: sequencing))
    • CeGaT GmbH
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of benign familial neonatal-infantile seizures (SCN2A gene: sequencing)
    • CeGaT GmbH
    • More information
    • FRANCE
    • RHONE-ALPES
    • LYON
    • Molecular diagnosis of benign familial neonatal-infantile seizures (SCN2A gene)
    • CHRU Lyon - Hôpital Edouard Herriot
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular diagnosis of generalized epilepsy with febrile seizures plus (GABRD, GABRG2, SCN1A, SCN1B, SCN2A genes)
    • Praxis Dres. Gencik
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular diagnosis of benign familial neonatal-infantile seizures (SCN2A gene)
    • Praxis Dres. Gencik
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of benign familial infantile seizures (SCN2A gene)
    • Praxis für Humangenetik
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • Molecular diagnosis of Dravet syndrome / GEFS+ type 2 (SCN1A, SCN2A, SCN1B genes)
    • Institut für Klinische Genetik Bonn
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • Molecular diagnosis of generalized epilepsy with febrile seizures plus (SCN1A and SCN2A genes)
    • Institut für Klinische Genetik Bonn
    • More information
    • GERMANY
    • Baden-Württemberg
    • ULM
    • Molecular diagnosis of benign familial neonatal-infantile seizures (SCN2A gene)
    • Universität Ulm
    • More information
    • DENMARK
    • Fyn
    • ODENSE
    • Molecular diagnosis of generalized epilepsy with febrile seizures-plus context (GABRG2, SCN1A, SCN1B and SCN2A gene sequencing)
    • Amplexa Genetics A/S
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of generalized epilepsy with febrile seizures-plus context (deletions by MLPA analysis and entire coding sequence of SCN1A gene; entire coding sequence of SCN1B, SCN2A, GABRD and GABRG2 genes)
    • LABORATORIO DE GENÉTICA CLÍNICA S.L.
    • More information