Erratum
Unfortunately, after publication of the original version of this article [1], it was noticed that there were some errors in Fig. 3 and Fig. 4:
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In Fig. 3, the methylation of H19/IGF2:IG-DMR hypomethylation is not correctly illustrated: the lolly pops should be empty (=unmethylated).
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In Fig. 4, the methylation of both H19/IGF2:IG-DMR hypermethylation and KCNQ1OT1:TSS-DMR hypomethylation are not correctly illustrated: in case of the H19/IGF2:IG-DMR hypermethylation the lolly pops should be filled (=methylated), and for the KCNQ1OT1:TSS-DMR, they should be empty (=unmethylated).
The corrected Fig. 3 and Fig. 4 have been included in this erratum.
Reference
Eggermann T, Perez de Nanclares G, Maher ER, Temple IK, Tümer Z, Monk D, et al. Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci. Clin Epigenetics. 2015;7:123. doi:10.1186/s13148-015-0143-8.
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The online version of the original article can be found under doi:10.1186/s13148-015-0143-8.
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Eggermann, T., de Nanclares, G.P., Maher, E.R. et al. Erratum to: Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci. Clin Epigenet 8, 27 (2016). https://doi.org/10.1186/s13148-016-0194-5
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DOI: https://doi.org/10.1186/s13148-016-0194-5