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

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

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

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

Research output: Contribution to conference › Poster › Other research output

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
Original language	Undefined/Unknown
Publication status	Published - 23 Apr 2009
Event	NVHG voorjaarsymposium - Veldhoven Duration: 23 Apr 2009 → 24 Apr 2009

Conference

Conference	NVHG voorjaarsymposium
City	Veldhoven
Period	23/04/09 → 24/04/09

Keywords

Econometric and Statistical Methods: General
Geneeskunde(GENK)

Cite this

@conference{f8e818eca7084641afd2f9eac8f6720c,

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

keywords = "Econometric and Statistical Methods: General, Geneeskunde(GENK)",

author = "A. Buijs and {van Binsbergen}, E. and M.G.E.M. Ausems and M. Poot and M.B. Bierings and {van der Crabben}, S.N.",

note = "NVHG voorjaarsymposium; NVHG voorjaarsymposium ; Conference date: 23-04-2009 Through 24-04-2009",

year = "2009",

month = apr,

day = "23",

language = "Undefined/Unknown",

}

Non-syndromic constitutional RUNX1 deletion presenting as thrombocytopenia with myelodysplasia; implications for ITSN1 as a 21q candidate gene in mental retardation. / Buijs, A.; van Binsbergen, E.; Ausems, M.G.E.M. et al.
2009. Poster session presented at NVHG voorjaarsymposium, Veldhoven.

Research output: Contribution to conference › Poster › Other research output

TY - CONF

T1 - Non-syndromic constitutional RUNX1 deletion presenting as thrombocytopenia with myelodysplasia; implications for ITSN1 as a 21q candidate gene in mental retardation

AU - Buijs, A.

AU - van Binsbergen, E.

AU - Ausems, M.G.E.M.

AU - Poot, M.

AU - Bierings, M.B.

AU - van der Crabben, S.N.

N1 - NVHG voorjaarsymposium

PY - 2009/4/23

Y1 - 2009/4/23

KW - Econometric and Statistical Methods: General

KW - Geneeskunde(GENK)

M3 - Poster

T2 - NVHG voorjaarsymposium

Y2 - 23 April 2009 through 24 April 2009

ER -