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Autori: Horsthemke Bernhard

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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 
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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