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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 21, 2004
Genetic insights into familial tumors of the nervous systemGerman Melean, Roberta Sestini, Franco Ammannati, et al.Genetic Testing|April 29, 2005
Detection of rearrangements in the NF2 gene using semi-quantitative multiplex fluorescent PCRRoberta Sestini, Anna Laura Putignano, Franco Ammannati, et al.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.European Journal of Obstetrics, Gynecology, and Reproductive Biology|January 30, 2004
Premature ovarian failure and fragile X premutation: a study on 45 womenCecilia Bussani, Laura Papi, Roberta Sestini, et al.The Journal of Molecular Diagnostics : JMD|May 13, 2014
Application of COLD-PCR for improved detection of NF2 mosaic mutationsIrene Paganini, Irene Mancini, Marta Baroncelli, et al.Journal of Neuro-Oncology|December 13, 2017
Double somatic SMARCB1 and NF2 mutations in sporadic spinal schwannomaIrene Paganini, Gabriele Lorenzo Capone, Jeremie Vitte, et al.BMC Cancer|July 23, 2011
High resolution melting analysis for a rapid identification of heterozygous and homozygous sequence changes in the MUTYH geneRossella Tricarico, Francesca Crucianelli, Antonio Alvau, et al.The Journal of Molecular Diagnostics : JMD|July 10, 2010
The use of COLD-PCR and high-resolution melting analysis improves the limit of detection of KRAS and BRAF mutations in colorectal cancerIrene Mancini, Claudio Santucci, Roberta Sestini, 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 3