Kongenitale Schwerhörigkeit
Author:
Publisher
Springer Science and Business Media LLC
Subject
Otorhinolaryngology
Link
http://link.springer.com/content/pdf/10.1007/s00106-004-1159-0.pdf
Reference24 articles.
1. Angeli S, Utrera R, Dib S, Chiossone E, Naranjo C, Henriquez O, Porta M (2000) GJB2 gene mutations in childhood deafness. Acta Otolaryngol 120: 133–136
2. Van Camp G, Smith RJH (2004) Hereditary Hearing Loss Homepage.http:/dnalab-www.uia.ac.be/dnalab/hhh
3. Denoyelle F, Weil D, Maw MA et al. (1997) Prelingual deafness: high prevalence of a c.35delG Mutation in the connexin 26 gene. Hum Mol Genet 6: 24–28
4. Gabriel H, Kupsch P, Sudendey J, Winterhager E, Jahnke K, Lautermann J (2001) Mutations in the Connexin 26/GJB2 Gene are the most common event in non-syndromic hearing loss among the German population. Hum Mutat 17: 521–522
5. Kupka S, Mirghomizadeh F, Haug T et al. (2000) Muationsanalyse des Connexin-26-Gens bei sporadischen Fällen mittels- bis hochgradiger Schwerhörigkeit. HNO 48: 671–674
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1. Extended Preoperative Audiometry for Outcome Prediction and Risk Analysis in Patients Receiving Cochlear Implants;Journal of Clinical Medicine;2023-05-03
2. GJB2-associated hearing loss: Systematic review of worldwide prevalence, genotype, and auditory phenotype;The Laryngoscope;2013-10-08
3. Neurogene Stammzelltransplantation in die Kochlea;HNO;2007-05-09
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