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Browsing by Author Siebert, Reiner
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| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2016 | A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith–Wiedemann syndrome | Beygo, Jasmin; Joksić, Ivana; Strom, Tim M.; Lüdecke, Hermann-Josef; Kolarova, Julia; Siebert, Reiner; Miković, Željko   ; Horsthemke, Bernhard; Buiting, Karin | Article | 21M21 |
| 2010 | Possible Genetic Heterogeneity of Spinocerebellar Ataxia Linked to Chromosome 15 | Weissbach, Anne; Djarmati, Ana; Klein, Christine; Dragasevic, Natasa ; Zuehlke, Christine; Rakovic, Aleksandar; Gužvić, Miodrag ; Butz, Elisabeth; Toennies, Holger; Siebert, Reiner;
Petrović, Igor
; Svetel, Marina ; Kostic, Vladimir S. ; Lohmann, Katja; | Article | 21aM21a |