Novel 3q26 EVI1/MECOM deletion syndrome in a newborn with multiple severe congenital abnormalities and bone marrow failure

Translated title of the contribution: Novel 3q26 EVI1/MECOM deletion syndrome in a newborn with multiple severe congenital abnormalities and bone marrow failure

L.T.J.N. van der Veken, M.B. Bierings, M.C. Maiburg, F. Groenendaal, A.C. Bloem, N.V.A.M. Knoers, A. Buijs

Research output: Contribution to conferencePosterOther research output

Translated title of the contributionNovel 3q26 EVI1/MECOM deletion syndrome in a newborn with multiple severe congenital abnormalities and bone marrow failure
Original languageUndefined/Unknown
Publication statusPublished - 13 Jun 2013
Event18th Congress of the European Hematology Association - Stockholm, Zweden
Duration: 13 Jun 201316 Jun 2013

Conference

Conference18th Congress of the European Hematology Association
CityStockholm, Zweden
Period13/06/1316/06/13

Keywords

  • Econometric and Statistical Methods: General
  • Geneeskunde (GENK)
  • Geneeskunde(GENK)
  • Medical sciences
  • Bescherming en bevordering van de menselijke gezondheid

Cite this