Associated Papers
Mosaicism in Tumor Suppressor Gene Syndromes: Prevalence, Diagnostic Strategies, and Transmission Risk.
Chen JL et al.
Annual Review of Genomics and Human Genetics, 2022
36044908 (PubMed )
Supplement: gg23-giannikou_suptable1.xlsx › NF2
NF2 genetic alterations in sporadic vestibular schwannomas: clinical implications.
Lassaletta L et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology, 2013
Microarray analysis of gene expression in vestibular schwannomas reveals SPP1/MET signaling pathway and androgen receptor deregulation.
Torres-Martin M et al.
International Journal of Oncology, 2013
NF2 mutation screening by denaturing high-performance liquid chromatography and high-resolution melting analysis.
Sestini R et al.
Genetic Testing, 2008
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