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Human Mutation|December 12, 2007
Evidence of a four-hit mechanism involving SMARCB1 and NF2 in schwannomatosis-associated schwannomasRoberta Sestini, Costanza Bacci, Aldesia Provenzano, et al.Genetic Testing|June 17, 2008
NF2 mutation screening by denaturing high-performance liquid chromatography and high-resolution melting analysisRoberta Sestini, Aldesia Provenzano, Costanza Bacci, et al.Cancers|December 17, 2024
Alu-Mediated Duplication and Deletion of Exon 11 Are Frequent Mechanisms of PALB2 Inactivation, Predisposing Individuals to Hereditary Breast-Ovarian Cancer SyndromeDiletta Sidoti, Valeria Margotta, Diletta Calosci, et al.Neurogenetics|July 8, 2009
Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutationCostanza Bacci, Roberta Sestini, Aldesia Provenzano, et al.Pageof 1