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Caption : Accreditation =Accreditation
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    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Multiple Congenital Anomalies (SNP-array)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Unexplained Intellectual Deficit with Multiple Congenital Anomalies (SNP-array)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • UNITED KINGDOM
    • Oxfordshire
    • OXFORD
    • Accreditation
    • Molecular diagnosis of Mitochondrial diseases (common mtDNA point mutations, mtDNA rearrangements and depletion)
    • The Churchill Hospital
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Accreditation
    • Molecular diagnosis of autosomal dominant optic atrophy (OPA1 gene) : genotyping by arrayed primer extension (APEX)
    • Asper Biotech Ltd.
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of ectodermal dysplasia (EDA, NFKBIA, GJB6, EDAR, and EDARADD genes)
    • Praxis für Humangenetik
    • More information
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • Molecular diagnosis of mitochondrial diseases (mtDNA/POLG/Twinkle)
    • Karolinska University Hospital - Solna
    • More information
    • ITALY
    • CALABRIA
    • MANGONE
    • ITALY
    • TRENTINO ALTO ADIGE
    • ROVERETO
    • Molecular diagnosis of optic atrophy (OPA1 gene)
    • MAGI'S LAB srl
    • More information