eNauka - pregled
Pregled prema Autor Siebert, Reiner
Prikaz rezultata 1 do 2 od 2
| Godina | Naslov | Autor(i) | Tip rezultata | Mp-kat. |
|---|---|---|---|---|
| 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 |