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2. Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss
作者：Sandra Iossa (1) (2)
Valerio Costa (3)
Virginia Corvino (4)
Gennaro Auletta (4)
Luigi Barruffo (4)
Stefania Cappellani (5)
Carlo Ceglia (2)
Giovanni Cennamo (6)
Adamo Pio D鈥橝damo (5) (7)
Alessandra D鈥橝mico (8)
Nilde Di Paolo (8)
Raimondo Forte (9)
Paolo Gasparini (5) (7)
Carla Laria (4)
Barbara Lombardo (1) (2)
Rita Malesci (4)
Andrea Vitale (10)
Elio Marciano (4)
Annamaria Franz猫 (2) (4)

1. DMMBM ; Universit脿 di Napoli 鈥淔ederico II鈥? Naples ; Italy
2. Ceinge Biotecnologie Avanzate ; Naples ; Italy
3. IGB 鈥淎. Buzzati Traverso鈥? CNR ; Naples ; Italy
4. Istituto di Audiologia ; Dipartimento di Neuroscienze ; Scienze Riproduttive e Odontostomatologiche ; Universit脿 di Napoli 鈥淔ederico II鈥? Naples ; Italy
5. Institute for Maternal and Child Health - IRCCS 鈥淏urlo Garofolo鈥? Trieste ; Italy
6. Dipartimento di Oftalmologia ; Universit脿 di Napoli 鈥淔ederico II鈥? Naples ; Italy
7. University of Trieste ; Trieste ; Italy
8. Dipartimento di Scienze Biomediche Avanzate ; Universit脿 di Napoli 鈥淔ederico II鈥? Naples ; Italy
9. Dipartimento di Oftalmologia Pediatrica ; Universit脿 di Salerno ; Salerno ; Italy
10. Dipartimento di Scienze Motorie e del Benessere ; Universit脿 di Napoli 鈥淧arthenope鈥? Naples ; Italy
刊名：Molecular Cytogenetics
出版年：2015
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