| Titolo | Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss. |
| Publication Type | Journal Article |
| Authors | Iossa, S, Costa, V, Corvino, V, Auletta, G, Barruffo, L, Cappellani, S, Ceglia, C, Cennamo, G, d'Adamo, APio, D'Amico, A, Di Paolo, N, Forte, R, Gasparini, P, Laria, C, Lombardo, B, Malesci, R, Vitale, A, Marciano, E, Franzè, A |
| PubMed ID | 25821518 |
| PubMed Central ID | PMC4376344 |