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About this Medicine article
Elucidation of a novel pathogenomic mechanism using genome-wide long mate-pair sequencing of a congenital t(16;21) in a series of three RUNX1-mutated FPD/AML pedigrees by Buijs, A; Poot, M; van der Crabben, S; van der Zwaag, B; van Binsbergen, E; van Roosmalen, M J; Tavakoli-Yaraki, M; de Weerdt, O; Nieuwenhuis, H K; van Gijn, M; Kloosterman, W P is a Medicine article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Medicine.
- Author
- Buijs, A; Poot, M; van der Crabben, S; van der Zwaag, B; van Binsbergen, E; van Roosmalen, M J; Tavakoli-Yaraki, M; de Weerdt, O; Nieuwenhuis, H K; van Gijn, M; Kloosterman, W P
- Publisher
- Nature Publishing Group; Springer Science and Business Media LLC (ISSN 0887-6924)
- Published
- 2012
- Field
- Medicine (Health Sciences)