Segmental uniparental disomy as a recurrent mechanism for homozygous CEBPA mutations in acute myeloid leukemia

Bas Wouters, Mathijs Sanders, Sanne Lugthart, WM Geertsma-Kleinkoort, E Drunen, Berna Beverloo, Bob Löwenberg, Peter Valk, Ruud Delwel

Research output: Contribution to journalArticleAcademicpeer-review

23 Citations (Scopus)
Original languageUndefined/Unknown
Pages (from-to)2382-2384
Number of pages3
JournalLeukemia
Volume21
DOIs
Publication statusPublished - 2007

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