Publications by authors named "Luigi Barruffo"

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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, Gennaro Auletta, Luigi Barruffo

Mol Cytogenet· March 2015

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Feasibility and effectiveness of a population-based newborn hearing screening in an economically deprived region of Italy.
Alfredo Pisacane, Gennaro Auletta, Fabiana Toscano, Monica Errichiello, Francoise Barrier, Luigi Barruffo

Int J Pediatr Otorhinolaryngol· March 2013

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