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SNP array analysis of leukemic relapse samples after allogeneic hematopoietic stem cell transplantation with a sibling donor identifies meiotic recombination spots and reveals possible correlation with the breakpoints of acquired genetic aberrations

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Acknowledgements

This work was supported by grants from the Swedish Childhood Cancer Foundation, the Swedish Cancer Fund, the Swedish Society for Medical Research, and the Swedish Research Council.

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Correspondence to K Paulsson.

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Paulsson, K., Lindgren, D. & Johansson, B. SNP array analysis of leukemic relapse samples after allogeneic hematopoietic stem cell transplantation with a sibling donor identifies meiotic recombination spots and reveals possible correlation with the breakpoints of acquired genetic aberrations. Leukemia 25, 1358–1361 (2011). https://doi.org/10.1038/leu.2011.79

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