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. 2015 Apr 21;7(1):48. doi: 10.1186/s13148-015-0081-5

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© Rezwan et al.; licensee BioMed Central. 2015

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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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Identification of hypomethylation at the SNRPN locus in MLMD samples. Upper panel: Genomic location from the UCSC genome browser, illustrating the SNRPN gene and the imprinting control region. Lower panel: graphical presentation of 450 k DNA methylation data across the SNRPN gene in BWS-MLMD 4 (red) and TND-MLMD 5 (blue). The x-axis corresponds to the genomic location as illustrated in the upper panel. The primary y-axis (left) represents the CH P value (solid lines); the secondary y-axis (right) represents the difference in M value between the cases and controls (dashed lines). BWS-MLMD, Beckwith-Wiedemann syndrome-multi-locus methylation disorders; TND-MLMD, transient neonatal diabetes-multi-locus methylation disorders.