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. 2018 Jun 26;18:136. doi: 10.1186/s12870-018-1308-3

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© The Author(s). 2018

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 3 — Validation of QTLs for δ¹³C under drought-stressed conditions, based on genotyping using KASP assay-based SNP markers. a genotype plot on 3 positions (lm1712, np2623, and np2691) for KASP platform. b phenotypic distribution of δ¹³C measured in HC × QG segregating population under drought-stressed conditions, based on 3 stable positions (lm1712, np2623, and np2691). lm, ll, nn, and np represent genotypes detected by RAD-SNP marker genotyping. Base pairs represent genotypes detected by KASP array. Significance levels of differences at p < 0.05 and p < 0.01 are indicated with “*” and “**”, respectively. c genotypes of 7 commercial apple cultivars on 3 stable positions (lm1712, np2623, and np2691), as detected by KASP assay. Phenotypic values of δ¹³C in several cultivars under drought-stressed conditions were reported by Liu et al. [28]