A genotype–phenotype correlation in Sicilian patients with GJB2 biallelic mutations-Reference-Cited by-同舟云学术

A genotype–phenotype correlation in Sicilian patients with GJB2 biallelic mutations

Published:2014-03-14 Issue:8 Volume:272 Page:1857-1865
ISSN:0937-4477
Container-title:European Archives of Oto-Rhino-Laryngology
language:en
Short-container-title:Eur Arch Otorhinolaryngol

Author:

Martines Francesco,Salvago Pietro,Bartolotta Caterina,Cocuzza Salvatore,Fabiano Carmelo,Ferrara Sergio,La Mattina Eleonora,Mucia Marianna,Sammarco Pietro,Sireci Federico,Martines Enrico

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Otorhinolaryngology

Link

http://link.springer.com/content/pdf/10.1007/s00405-014-2970-1.pdf

Reference36 articles.

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2. Martines F, Porrello M, Ferrara M, Martines M, Martines E (2007) Newborn hearing screening project using transient evoked otoacoustic emissions: Western Sicily experience. Int J Pediatr Otorhinolaryngol 71:107–112

3. Martines F, Bentivegna D, Ciprì S, Costantino C, Marchese D et al (2012) On the threshold of effective well infant nursery hearing screening in Western Sicily. Int J Pediatr Otorhinolaryngol 76:423–427

4. Tekin M, Arons KS, Pandya A (2001) Advances in hereditary deafness. Lancet 358:1082–1090

5. Kenneson A, Van Naarden Braun K, Boyle C (2002) GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: a HuGE review. Genet Med 4:258–274

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