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Non-syndromic constitutional RUNX1 deletion presenting as thrombocytopenia with myelodysplasia; implications for ITSN1 as a 21q candidate gene in mental retardation

Translated title of the contribution: Non-syndromic constitutional RUNX1 deletion presenting as thrombocytopenia with myelodysplasia; implications for ITSN1 as a 21q candidate gene in mental retardation

Research output: Contribution to conferencePosterOther research output

Translated title of the contributionNon-syndromic constitutional RUNX1 deletion presenting as thrombocytopenia with myelodysplasia; implications for ITSN1 as a 21q candidate gene in mental retardation
Original languageUndefined/Unknown
Publication statusPublished - 4 Jul 2009
Event7th European Cytogenetics Conference - Stockholm, Sweden
Duration: 4 Jul 20097 Jul 2009

Conference

Conference7th European Cytogenetics Conference
CityStockholm, Sweden
Period4/07/097/07/09

Keywords

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

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