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. 2016 Mar 1;8:23. doi: 10.1186/s13148-016-0183-8

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© Russo et al. 2016

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 — SNP array Bead Studio output of selected BWS borderline cases. All the indicated BWS patients, “suspected” by microsatellite 11p15 analysis, are confirmed to carry a mosaic segmental paternal uniparental disomy (upd(11)pat). Patients are listed from top to bottom according to decreasing extent of the mosaic isodisomy (framed in red in the ideogram below each profile). The percentage of upd(11)pat in the DNA from blood cells, calculated from the array data as described (see the “Methods” section), ranges from 20 % (BWS-15, BWS-21) to 15 % (BWS-14) down to 10 % (BWS-12, BWS-13, and BWS-16)