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Original Article

Application of the Audioscan in the Detection of Carriers of Genetic Hearing Loss

Original Paper

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Pages 91-97 | Received 09 Nov 1994, Accepted 06 Apr 1995, Published online: 07 Jul 2009

References

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  • Anderson H, Wedenberg E. Audiometric identification of normal hearing carriers of genes for deafness. Acta Otolaryngol 1968; 65: 535–554
  • Taylor I G, Hine W D, Brasier V J, Chiveralls K, Morris T. A study of the causes of hearing loss with special reference to genetic factors. J LaryngolOtol 1975; 89: 899–914
  • Meyer-Bisch C. Audiomérie auto-matique de dépistage préventif: Le balayage fréquentiel asservi (Au-dioscan). Cah Notes Document 1990; 139: 335–345
  • Meredith R, Stephens D, Meyer-Bisch C, Reardon W, Sirimanna T. Audiometric detection of carriers of Usher's syndrome type II. J Audiol Med 1992; 1: 11–19
  • Sirimanna K S, France E, Stephens S DG. Alport's syndrome: Can the carrier be identified by audiometry. Clin Otolaryngol 1995; 20: 158–163
  • Meredith R. Audiometric identification of carriers of non-manifesting genes for deafness; MSc thesis. Southampton 1991
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  • Almqvist C, Haugen H. Audiometric notches - An indication of recessive genetic deafness; preclin Diss, Lund 1992
  • France E A, Stephens S DG. The All-Wales Audiology and Genetic Service for Hearing Impaired Young Adults. J Audiol Med, (in press)
  • Harper P S. Practical genetic counselling, ed. 4. Wright, London 1991

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