Media type: E-Article Title: A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith–Wiedemann syndrome Contributor: Beygo, Jasmin; Joksic, Ivana; Strom, Tim M; Lüdecke, Hermann-Josef; Kolarova, Julia; Siebert, Reiner; Mikovic, Zeljko; Horsthemke, Bernhard; Buiting, Karin Published: Springer Science and Business Media LLC, 2016 Published in: European Journal of Human Genetics, 24 (2016) 9, Seite 1280-1286 Language: English DOI: 10.1038/ejhg.2016.3 ISSN: 1018-4813; 1476-5438 Keywords: Genetics (clinical) ; Genetics Origination: Footnote: Access State: Open Access