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Original Article

Dips on Békésy or Audioscan Fail to Identify Carriers of Autosomal Recessive Non-Syndromic Hearing Loss

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Pages 521-527 | Received 26 Jun 1995, Accepted 05 Oct 1995, Published online: 08 Jul 2009

References

  • Anderson H, Wedenberg E. Audiometric identification of normal hearing carriers of genes for deafness. Acta Otolaryngol (Stockh) 1968; 65: 535–54
  • Parving A. Reliability of Békésy threshold tracing in identification of carriers of genes for an x-linked disease with deafness. Acta Otolaryngol (Stockh) 1978; 85: 40–4
  • Marres H AM, Cremers C WRJ. Autosomal recessive nonsyndromal profound childhood deafness in a large pedigree. Audiometric features of the affected persons and the obligate carriers. Arch Otolaryngol Head Neck Surg 1989; 115: 591–5
  • Meyer-Bisch C. Audiometrie automatique de depist-age preventif: le balayage freqential asservi (au-dioscan). Cahiers de Notes Documentaires 1990; 139: 335–45
  • 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: 11–9
  • Liu X Z, Xu L. Nonsyndromic hearing loss: an analysis of audiograms. Ann Otol Laryngol 1994; 103: 428–33
  • Morton NE. Genetic epidemiology of hearing impairment. Genetics of hearing impairment., R J Ruben, T R Van De Water, KP Steel. New York Academy of Science, New York 1991; 630: 16–31
  • Stephens D, Meredith R, Sirimanna T, France L, Almqvist C, Haugen H. Application of the audioscan in the detection of carriers of genetic hearing loss. Audiology 1995; 34: 91–7
  • Sirimanna T. Identification of carriers of Alport's syndrome by audiometry. MSc thesis. Manchester 1993
  • Meredith R. Audiometric identification of carriers of non-manifesting genes for deafness. MSc thesis. Southampton 1991

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