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A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith–Wiedemann syndrome
| Naziv: | A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith–Wiedemann syndrome | Autori: | Beygo, Jasmin; Joksić, Ivana; Strom, Tim M.; Lüdecke, Hermann-Josef; Kolarova, Julia; Siebert, Reiner; Miković, Željko   ; Horsthemke, Bernhard; Buiting, Karin |
Godina: | 2016 | Publikacija: | European journal of human genetics | ISSN: | 1018-4813 European Journal of Human Genetics Pretraži identifikator |
Izdavač: | London : Nature Publishing Group | Tip rezultata: | Naučni članak | Kolacija: | vol. 24 br. 9 str. 1280-1286 | DOI: | 10.1038/ejhg.2016.3 | WoS-ID: | 000382310600008 | Scopus-ID: | 2-s2.0-84956928161 | PMID: | 26839037 | PMCID: | PMC4989213 | URI: | https://enauka.gov.rs/handle/123456789/518424 | URL: | https://www.nature.com/articles/ejhg20163 | Izvor metapodataka: | Migrirano iz RIS podataka | M-kategorija: | 21M21 - Vodeći međunarodni časopis kategorije M21 |
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