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    • Home
    • Diagnostics
      • Polycythemia Vera
      • Essential Thrombocythemia
      • Primary Myelofibrosis
      • Congenital Erythrocytosis
      • Hereditary Thrombocytosis
    • Molecular analyses
      • JAK2V617F
      • JAK2 Exon 12 mutations
      • Mpl/TPO_Receptor
      • Calreticulin (CALR)
      • Other genes mutated in MPN
      • EPO-Receptor
      • Oxygen sensing pathway genes
      • THPO
    • Events
    • Useful links
    • Members
    • Registration
    • INTRANET

      Events

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      • Coimbra, Portugal – October 2011

      Coimbra, Portugal – October 2011

      EVENT DESCRIPTION

      Molecular Diagnosis of Congenital Erythrocytosis

      EVENT CONTENT

      • To get the latest information on the different mutations leading to congenital erythrocytosis.
      • To acquire competences in the various techniques used for the molecular diagnosis of congenital erythrocytosis. The training school is organized in two sessions (see programme):
        • Morning plenary session/lectures: theory.
        • Afternoon practical session: applicants will perform the different assays, assisted by experts, and analyze the results.
      • To start a cooperative group which could share samples, reference materials and hopefully, generate original studies.

      MORE INFORMATIONS

      Start Time

      7:00 pm

      October 20, 2011

      Finish Time

      1:00 pm

      October 22, 2011

      Address

      Av. Afonso Romão Coimbra - Portugal

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      Former EU-sponsored COST Action BM0902 (2009-2013), a network of experts … “

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