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Caption : Accreditation =Accreditation
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    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular diagnosis of Feingold syndrome (MYCN gene: sequencing)
    • Bioscientia Institut für Medizinische Diagnostik GmbH
    • More information
    • UNITED KINGDOM
    • Devon
    • EXETER
    • Accreditation
    • Molecular diagnosis of Feingold Syndrome 1 by sequencing of the entire coding region of gene(s) (MYCN gene)
    • Royal Devon and Exeter Hospital - Wonford site
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular diagnosis of Feingold syndrome (MYCN gene)
    • Zentrum für Humangenetik Mannheim
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • SCHLIEREN
    • Accreditation
    • Search of genomic DNA duplications and/or deletions by CGH arrays
    • Universität Zürich
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of Feingold Syndrome (MYCN gene)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Multiple Congenital Anomalies (SNP-array)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of Feingold syndrome (MIR17HG, MYCN genes)
    • Praxis für Humangenetik Freiburg
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular genetic diagnosis of Feingold syndrome (MYCN and MIR17HG genes)
    • CHU Paris - Hôpital Necker-Enfants Malades
    • More information
    • FRANCE
    • HAUTE-NORMANDIE
    • ROUEN
    • Molecular cytogenetic diagnosis of Feingold syndrome
    • CHU de Rouen - Hôpital Charles Nicolle
    • More information
    • ITALY
    • LIGURIA
    • GENOVA
    • Molecular diagnosis of brachydactyly type E (HOXD13 gene)
    • Ospedali Galliera
    • More information
    • SPAIN
    • País Vasco
    • SAN SEBASTIÁN
    • Molecular diagnosis of Feingold syndrome (MYCN gene / array-CGH)
    • Policlínica Gipuzkoa
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Feingold syndrome (MYCN gene: sequencing of the entire coding region, FISH and deletion/duplication analysis by MLPA)
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular diagnosis of Feingold syndrome (MYCN gene / entire coding sequence)
    • Centro Inmunológico de Alicante (CIALAB)
    • More information
    • POLAND
    • Poznan
    • POZNAN
    • Molecular diagnosis of Feingold syndrome (MYCN gene: analysis of coding region)
    • NZOZ Centrum Genetyki Medycznej Genesis
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • SPAIN
    • País Vasco
    • DERIO
    • Molecular diagnosis of Feingold syndrome (aCGH)
    • Genetadi Biotech S.L.
    • More information