| Translated title of the contribution | Constitutional RUNX1 deletion presenting as non-syndromic thrombocytopenia with myelodysplasia: 21q22 ITSN1 as a candidate gene in mental retardation |
|---|---|
| Original language | Undefined/Unknown |
| Pages (from-to) | 8-12 |
| Number of pages | 5 |
| Journal | Leukemia Research |
| Volume | 31 |
| Issue number | 4 |
| Publication status | Published - 2010 |
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. Ausems, M. Poot, M. Bierings, A. Buijs
Research output: Contribution to journal › Article › Academic › peer-review