Deep exploration of a CDKN1C mutation causing a mixture of Beckwith-Wiedemann and IMAGe syndromes revealed a novel transcript associated with developmental delay

Autor:	Berland, Siren, Haukanes, Bjørn Ivar, Juliusson, Petur Benedikt, Houge, Gunnar
Databáze:	NORA (Norwegian Open Research Archive)
Externí odkaz:	https://hdl.handle.net/11250/3025751 Zobrazit plný text záznamu