Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss
Sandra Iossa(CEINGE Biotecnologie Avanzate Franco Salvatore (Italy)), Annamaria Franzè(CEINGE Biotecnologie Avanzate Franco Salvatore (Italy)), Giovanni Cennamo(Federico II University Hospital), Raimondo Forte(Hôpital Intercommunal de Créteil), Gennaro Auletta(University of Naples Federico II), Elio Marciano(University of Naples Federico II), Andrea Vitale(Parthenope University of Naples), Alessandra D’Amico(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Valerio Costa(Institute of Genetics and Biophysics), Rita Malesci(Federico II University Hospital), Barbara Lombardo(CEINGE Biotecnologie Avanzate Franco Salvatore (Italy)), Luigi Barruffo(University of Naples Federico II), Stefania Cappellani(IRCCS Materno Infantile Burlo Garofolo), Carlo Ceglia(CEINGE Biotecnologie Avanzate Franco Salvatore (Italy)), Pio D’Adamo(University of Trieste), Carla Laria(University of Naples Federico II), Virginia Corvino(University of Naples Federico II), Nilde Di Paolo, Paolo Gasparini(Brigham and Women's Hospital)
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