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International Journal of Audiology|December 9, 2003
Otosclerosis: exclusion of linkage to the OTSC1 and OTSC2 loci in four Italian familiesFrancesca Di Leva, Adamo Pio D'Adamo, Luiaino Strollo, et al.
Audiology & Neuro-Otology|February 2, 2006
Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11)Francesca Di Leva, Pio D'Adamo, Maria Vittoria Cubellis, et al.
Audiology Research|February 21, 2017
Multicentre Evaluation of the Naída CI Q70 Sound Processor: Feedback from Cochlear Implant Users and ProfessionalsJeanette Martin, Christine Poncet-Wallet, Angelika Illg, et al.
Molecular Cytogenetics|March 31, 2015
Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing lossSandra Iossa, Valerio Costa, Virginia Corvino, et al.
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