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Audiological Findings in Williams Syndrome: A Study of 69 PatientsBAROZZI, Stefania; SOI, Daniela; CESARANI, Antonio et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 4, pp 759-771, issn 1552-4825, 13 p.Article

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A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processingSOLDA, Giulia; ROBUSTO, Michela; PRIMIGNANI, Paola et al.Human molecular genetics (Print). 2012, Vol 21, Num 3, pp 577-585, issn 0964-6906, 9 p.Article

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