Hair phenotype in non-syndromic deafness-Reference-Cited by-同舟云学术

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Hair phenotype in non-syndromic deafness

Published:2013-08 Issue:8 Volume:77 Page:1280-1285
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Volo T.,Sathiyaseelan T.,Astolfi L.,Guaran V.,Trevisi P.,Emanuelli E.,Martini A.

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference32 articles.

1. Prevalence of prelingual deafness in Italy;Bubbico;Acta Otorhinol. Italy,2007

2. Progress in understanding GJB2-linked deafness;Gualandi;Commun. Genet.,2003

3. Exploring the clinical and epidemiological complexity of GJB2-linked deafness;Gualandi;Am. J. Med. Genet.,2002

4. GJB2 mutations and degree of hearing loss: a multicenter study;Snoeckx Rl;Am. J. Hum. Genet.,2005

5. Occurrence of del(GIB6-D13S1830) mutation in Italian non-syndromic hearing loss patients carrying a single GJB2 mutated allele;Gualandi;Acta Otolaryngol.,2004

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Mapping pathogenic mutations suggests an innovative structural model for the pendrin (SLC26A4) transmembrane domain;Biochimie;2017-01

2. Connexins and pannexins in the integumentary system: the skin and appendages;Cellular and Molecular Life Sciences;2015-06-20

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