Autori: Siebert Reiner
| Naslov | A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndrome (Article) |
| Autori | Beygo Jasmin Joksic Ivana D  Strom Tim M Luedecke Hermann-Josef Kolarova Julia Siebert Reiner Mikovic Zeljko M Horsthemke Bernhard Buiting Karin
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| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2016), vol. 24 br. 9, str. 1280-1286 |
| Projekat | Bundesministerium fur Bildung und Forschung (BMBF) [01GM1513A, 01GM1513D] |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Possible Genetic Heterogeneity of Spinocerebellar Ataxia Linked to Chromosome 15 (Article) |
| Autori | Weissbach Anne Djarmati Ana Klein Christine Dragasevic Natasa T Zuehlke Christine Rakovic Aleksandar Guzvic Miodrag Butz Elisabeth Toennies Holger Siebert Reiner Petrovic Igor N Svetel Marina V Kostic Vladimir S Lohmann Katja
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| Info | MOVEMENT DISORDERS, (2010), vol. 25 br. 11, str. 1577-1582 |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science |
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