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

Saskia van der Crabben; Ellen van Binsbergen; Margreet Ausems; Martin Poot; Marc Bierings; Arjan Buijs

doi:https://doi.org/10.1016/j.leukres.2009.06.030

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

Saskia van der Crabben, Ellen van Binsbergen, Margreet Ausems, Martin Poot, Marc Bierings, Arjan Buijs

Research output: Contribution to journal › Article › Academic › peer-review

30 Citations (Scopus)

Original language	English
Pages (from-to)	e8
Journal	Leukemia research
Volume	34
Issue number	1
DOIs	https://doi.org/10.1016/j.leukres.2009.06.030
Publication status	Published - Jan 2010

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

author = "{van der Crabben}, Saskia and {van Binsbergen}, Ellen and Margreet Ausems and Martin Poot and Marc Bierings and Arjan Buijs",

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AU - Ausems, Margreet

AU - Poot, Martin

AU - Bierings, Marc

AU - Buijs, Arjan

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

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