Gennaro Auletta

Enlarged vestibular aqueduct and Mondini Malformation: audiological, clinical, radiologic and genetic features

Francesca Forlì, Francesco Lazzerini, Gennaro Auletta et al. · European Archives of Oto-Rhino-Laryngology · 2020 · 35 citations · Full text

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 and Neurotology · 2006 · 30 citations

New evidence for the correlation of the p.G130V mutation in the <i>GJB2</i> gene and syndromic hearing loss with palmoplantar keratoderma

Sandra Iossa, Viviana Chinetti, Gennaro Auletta et al. · American Journal of Medical Genetics Part A · 2008 · 24 citations

Syndromic Hearing Loss, Genetics, Genetic Epidemiology +16

Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss

Sandra Iossa, Valerio Costa, Virginia Corvino et al. · Molecular Cytogenetics · 2015 · 22 citations · Full text

Feasibility and effectiveness of a population-based newborn hearing screening in an economically deprived region of Italy

Alfredo Pisacane, Gennaro Auletta, F Toscano et al. · International Journal of Pediatric Otorhinolaryngology · 2013 · 21 citations

Early Diagnosis, Hearing Intervention, Pediatric Audiology +12