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Melanoma Research|November 10, 2007
The p.G23S CDKN2A founder mutation in high-risk melanoma families from Central ItalyFrancesca Gensini, Roberta Sestini, Mauro Piazzini, et al.European Journal of Human Genetics : EJHG|October 23, 2014
Expanding the mutational spectrum of LZTR1 in schwannomatosisIrene Paganini, Vivian Y Chang, Gabriele L Capone, et al.Melanoma Research|November 18, 2008
Genomic rearrangements of the CDKN2A locus are infrequent in Italian malignant melanoma families without evidence of CDKN2A/CDK4 point mutationsMarina Vignoli, Maria Chiara Scaini, Paola Ghiorzo, et al.Human Molecular Genetics|August 9, 2006
Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastomaPaola Ghiorzo, Sara Gargiulo, Lorenza Pastorino, et al.Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|April 3, 2017
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomasRosario Caltabiano, Gaetano Magro, Agata Polizzi, et al.Acta Neuropathologica|October 7, 2020
Epigenomic, genomic, and transcriptomic landscape of schwannomatosisSheila Mansouri, Suganth Suppiah, Yasin Mamatjan, et al.Pageof 3