Browsing Centre for Endocrinology by Author "Occhi, G"
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A Novel Mutation in the Upstream Open Reading Frame of the CDKN1B Gene Causes a MEN4 Phenotype
Occhi, G; Regazzo, D; Trivellin, G; Boaretto, F; Ciato, D; Bobisse, S; Ferasin, S; Cetani, F; Pardi, E; Korbonits, M (2013-03) -
Polymorphism or mutation? - The role of the R304Q missense AIP mutation in the predisposition to pituitary adenoma
Mothojakan, NB; Ferrau, F; Dang, MN; Barlier, A; Chanson, P; Occhi, G; Daly, AF; Schofl, C; Dal, J; Gadelha, MR (2016-10-14)