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Caption : Accreditation =Accreditation
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    • FRANCE
    • PROVENCE-ALPES-COTE D'AZUR
    • MARSEILLE
    • Accreditation
    • Molecular diagnosis of Hereditary sensory and autonomic neuropathy type 1 (SPTLC1 gene)
    • CHU de Marseille - Hôpital de la Timone
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of hereditary motor and sensory neuropathy type 1 (ATL1, DNMT1, SPTLC1, SPTLC2 genes)
    • Medizinisch Genetisches Zentrum München
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • ZÜRICH
    • Accreditation
    • Molecular diagnosis of hereditary motor and sensory neuropathy type 1 (SPTLC1 gene)
    • Genetica AG
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Accreditation
    • Molecular diagnosis of Hereditary sensory and autonomic neuropathy type 1A and 1C (SPTLC1 and SPTLC2 genes): sequencing of the entire coding region
    • Instituto de Biologia Molecular e Celular
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of hereditary motor and sensory neuropathy type 1 (ATL1 gene: sequencing / MLPA)
    • GenteQ GmbH
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular diagnosis of hereditary sensory and autonomic neuropathy HSAN1 (SPTLC1 gene)
    • Zentrum für Humangenetik Mannheim
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Hereditary Sensory and Autonomic Neuropathy HSAN1 (SPTLC1 gene)
    • National Hospital for Neurology and Neurosurgery
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Unexplained Metabolic Disorders (exome sequencing)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of Hereditary Sensory Neuropathy type 1E (DNMT1 gene)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of Hereditary Sensory and Autonomic Neuropathy type 1, 2 and 5 (SPTLC1, HSN2 and NGF gene)
    • AMC - Academisch Medisch Centrum
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of hereditary sensory and autonomic neuropathy HSAN1 (SPTLC1 gene: sequencing)
    • Praxis für Humangenetik Freiburg
    • More information
    • FRANCE
    • MIDI-PYRENEES
    • TOULOUSE
    • Accreditation
    • Molecular diagnosis of hereditary sensory and autonomic neuropathy type 1 (SPTLC1 and SPTLC2 genes)
    • CHU de Toulouse - Hôpital Purpan
    • More information
    • UNITED KINGDOM
    • Avon
    • BRISTOL
    • Accreditation
    • Molecular diagnosis of Hereditary Sensory and Autonomic Neuropathy HSAN1 (SPTLC1 gene)
    • Southmead Hospital
    • More information
    • GERMANY
    • Thüringen
    • JENA
    • Accreditation
    • Molecular diagnosis of hereditary motor and sensory neuropathy type 1 (ATL1, SPTLC1, SPTLC2 genes)
    • Institut für Humangenetik am Universitätsklinikum Jena
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of hereditary sensory and autonomic neuropathy type 1-5 (IKBKAP, NGF, NTRK1, SPTLC1 and WNK1 genes)
    • Centogene AG
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Accreditation
    • Molecular diagnosis of hereditary sensory and autonomic neuropathy type 1-5 (IKBKAP, NGF, NTRK1, SPTLC1 and WNK1 genes)
    • MVZ Fenner & Krasemann
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of hereditary sensory and autonomic neuropathy type 1 (SPTLC1 gene)
    • Sistemas Genómicos S.L.
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular diagnosis of hereditary sensory and autonomic neuropathy type 1-5 (IKBKAP(exon 19), NGF, NTRK1, SPTLC1(exon 5,6) and WNK1 genes)
    • Praxis Dres. Gencik
    • More information
    • PORTUGAL
    • SUL
    • LISBOA
    • Molecular diagnosis of hereditary motor and sensory neuropathy type 1 (SPTLC1 gene)
    • Faculdade de Medicina da Universidade de Lisboa
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of hereditary sensory and autonomic neuropathy (HSN1, HSN2, and NGFB genes)
    • Praxis für Humangenetik
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Hereditary sensory and autonomic neuropathy type 1A and 1C (SPTLC1 and SPTLC2 genes: sequencing of the entire coding region)
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Molecular diagnosis of hereditary sensory and autonomic neuropathy type 1-5 (IKBKAP, NGF, NTRK1, SPTLC1 and WNK1 genes)
    • Diagenom GmbH
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of hereditary sensory and autonomic neuropathy type 1 (SPTLC1 and SPTLC2 genes - entire coding sequence)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Molecular diagnosis of hereditary sensory and autonomic neuropathy HSAN1 (SPTLC1 gene: sequencing)
    • Gemeinschaftspraxis für Humangenetik
    • More information
    • CZECH REPUBLIC
    • Capital City Prague
    • PRAHA
    • Molecular diagnosis of hereditary sensory and autonomic neuropathy type 1 (SPTLC1 gene)
    • Motol university hospital - 2nd Medical School Charles University Prague
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of hereditary sensory and autonomic neuropathy, type 1 (SPTLC1 gene)
    • Mossakowski Medical Research Centre - Polish Academy of Sciances
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Biochemical diagnosis of inborn errors of metabolism (including Austrian newborn screening program for inborn errors of metabolism)
    • Medizinische Universität Wien
    • More information