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ГодинаНасловАутор(и)Тип резултатаМп-кат.
2015GeneYenta: A phenotype-based rare disease case matching tool based on online dating algorithms for the acceleration of exome interpretationGottlieb M M; Arenillas D J; Maithripala S; Maurerd Z D; Tarailo Graovac, Maja ; Armstrong L; Patel M; Van Karnebeek C; Wasserman W WКонференцијски рад
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2012Human pluripotent stem cell models of Fanconi Anaemia deficiency reveal an important role for Fanconi Anaemia proteins in cellular reprogramming and survival of haematopoietic progenitorsStojković, Miodrag ; Yung SK; Tilgner K; Ledran MH; Habibollah S; Neganova I; Singhapol C; Saretzki GC; Armstrong L; Przyborski SA;
Lako M.;
Article
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