Constitutional RUNX1 deletion presenting as non-syndromic thrombocytopenia with myelodysplasia: 21q22 ITSN1 as a candidate gene in mental retardation

Translated title of the contribution: Constitutional RUNX1 deletion presenting as non-syndromic thrombocytopenia with myelodysplasia: 21q22 ITSN1 as a candidate gene in mental retardation

S.N. van der Crabben, E. van Binsbergen, M.G.E.M. Ausems, M. Poot, M.B. Bierings, A. Buijs

Research output: Contribution to conferencePosterOther research output

Translated title of the contributionConstitutional RUNX1 deletion presenting as non-syndromic thrombocytopenia with myelodysplasia: 21q22 ITSN1 as a candidate gene in mental retardation
Original languageUndefined/Unknown
Publication statusPublished - 23 Apr 2009
EventVKGN Spring Symposium - Veldhoven
Duration: 23 Apr 200924 Apr 2009

Conference

ConferenceVKGN Spring Symposium
CityVeldhoven
Period23/04/0924/04/09

Keywords

  • Econometric and Statistical Methods: General
  • Geneeskunde(GENK)

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