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. 2021 Feb 27;11(2):42. doi: 10.1038/s41408-021-00434-2

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© The Author(s) 2021

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 2 — A Association of the combined genetic risk group with the incidence of severe chronic GVHD in the training cohort and validation cohort. B No difference could be observed between the genetic risk groups in patients with SEP in two consecutive cohorts (n = 144 and 159, respectively). C Association of serum CXCL9 levels at day +28 with the combined genetic risk group in patients without and with SEP. n.s. not significant; *P ≤ 0.05.