Iossa, S., Costa, V., Corvino, V., Auletta, G., Barruffo, L., Cappellani, S., . . . Franzè, A. (2015). Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss. Mol Cytogenet.

Iossa, Sandra, et al. "Phenotypic and Genetic Characterization of a Family Carrying Two Xq21.1-21.3 Interstitial Deletions Associated With Syndromic Hearing Loss." Mol Cytogenet 2015.

Iossa, Sandra, et al. "Phenotypic and Genetic Characterization of a Family Carrying Two Xq21.1-21.3 Interstitial Deletions Associated With Syndromic Hearing Loss." Mol Cytogenet 2015.