Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss. [1]
| 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 [2], Costa, V [3], Corvino, V [4], Auletta, G [5], Barruffo, L [6], Cappellani, S [7], Ceglia, C [8], Cennamo, G [9], d'Adamo, APio [10], D'Amico, A [11], Di Paolo, N [12], Forte, R [13], Gasparini, P [14], Laria, C [15], Lombardo, B [16], Malesci, R [17], Vitale, A [18], Marciano, E [19], Franzè, A [20] |
| PubMed ID | 25821518 [21] |
| PubMed Central ID | PMC4376344 |