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Caption : Accreditation =Accreditation
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    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Accreditation
    • Molecular diagnosis of autosomal dominant Robinow syndrome (WNT5A gene)
    • CHRU de Lille - Centre de Biologie Pathologie Génétique
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Accreditation
    • Search of genomic DNA duplications and/or deletions by array-CGH
    • Centre Hospitalier Universitaire Vaudois CHUV
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular diagnosis of autosomal dominant Robinow syndrome (WNT5A gene)
    • Zentrum für Humangenetik Mannheim
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • SCHLIEREN
    • Accreditation
    • Search of genomic DNA duplications and/or deletions by CGH arrays / chromosomal microarrays
    • Universität Zürich
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of Autosomal Dominant Robinow Syndrome (WNT5A 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
    • UNITED KINGDOM
    • Oxfordshire
    • OXFORD
    • Accreditation
    • Molecular diagnosis of autosomal dominant Robinow syndrome (WNT5A gene)
    • The Churchill Hospital
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of autosomal dominant Robinow syndrome (WNT5A gene)
    • Centogene AG
    • More information
    • FRANCE
    • BRETAGNE
    • BREST
    • Molecular diagnosis of dysmorphological syndromes by CGH array
    • CHRU de Brest - Hôpital Morvan
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular diagnosis of Robinow syndrome (ROR2, WNT5A genes / entire coding sequence)
    • Centro Inmunológico de Alicante (CIALAB)
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular diagnosis of Robinow syndrome (ROR2, WNT5A genes)
    • Genetaq
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of autosomal dominant Robinow syndrome (WNT5A gene / entire coding sequence)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Molecular diagnosis of autosomal dominant Robinow syndrome (WNT5A gene: sequencing)
    • Gemeinschaftspraxis für Humangenetik
    • More information