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Original Article

Reliability Of Békésy Threshold Tracing In Identification Of Carriers Of Genes For An X-Linked Disease With Deafness

Pages 40-44 | Received 08 Feb 1977, 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
  • Anderson H., Wedenberg E. Identification of normal hearing carriers of genes for deafness. Acta Otolaryngol (Stockh) 1976; 82: 245
  • Barr B., Anderson H., Wedenberg E. Epidemiology of hearing loss in childhood. Audiology 1973; 12: 426
  • Fraser G. R. Profound childhood deafness. J Med Genet 1964; 1: 118
  • Fraser G. R. Epidemiology of profound childhood deafness. Audiology 1974; 13: 335
  • Konigsmark B. W. Hereditary deafness in man. N Eng J Med 1969; 281: 713
  • Fraser G. R. Hereditary deafness syndromes with onset in adult life. Audiology 1971; 10: 257
  • Nance W. E. The principles and practice of genetic counseling. Ann Otol Rhinol Laryngol 1971; 80: 246
  • Nance W. E., Sweeney A. Genetic factors in deafness of early life. Otolaryngologic Clinics of North America 1975; 8(1)19
  • Parving A., Warburg M. Audiological findings in Nome's disease. Audiology 1977, In press
  • Siegenthaler B. M. Reliability of Békésy excursion size among normal adults. J Aud Res 1976; 15: 111
  • Warburg M. Norrie's disease. Acta Ophthalmol 1975; 53: 217
  • Wildervanck L. S. Audiometric examination of parents of children deaf from birth. Arch Otolaryngol 1957; 65: 280

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