Inherited and Sporadic Epimutations at the IGF2-H19 Locus in Beckwith-Wiedemann Syndrome and Wilms’ Tumor. In: Endocrine Involvement in Developmental Syndromes

Autor:	RICCIO A., SPARAGO A., VERDE G., DE CRESCENZO A., CITRO V., FERRERO G. B., CIRILLO SILENGO M., RUSSO S., LARIZZA L., CERRATO F., CUBELLIS, MARIA VITTORIA
Přispěvatelé:	Editor(s): Cappa, M. , Maghnie, M. Loche, S. Bottazzo, G.F. (Roma), Riccio, A., Sparago, A., Verde, G., DE CRESCENZO, A., Citro, V., Cubellis, MARIA VITTORIA, Ferrero, G. B., CIRILLO SILENGO, M., Russo, S., Larizza, L., Cerrato, F.
Rok vydání:	2008
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=od______3730::fab8a028dd7546c939aa722bd6a9de65 http://hdl.handle.net/11588/333004 Zobrazit plný text záznamu