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Audiology Volume 10, 1971 - Issue 5-6
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Original Article

Parental age - Birth order and congenital deafness

L. Fisch Institute of Laryngology and Otology, London
Pages 284-290 | Published online: 07 Jul 2009

References

  • Fisch L. Causes of congenital deafness. Publ. Hlth, Lond. 1969; 83: 68–74
  • Woolf B. On estimating the relation between blood groups and disease. Ann. hum. Genet. 1955; 19: 251–253
  • ANDERSON, H. and WEDENBERG, E. Audiometric identification of normal hearing carriers of genes for deafness. Acta oto-laryng., Stockh. 65: 535–554 (1968).
  • BASCHIERI, L.; BENEDETTI, G.; LUCA, F. DE, and NEGRI, M.: Evaluation and limitations of perchlorate test in the study of thyroid function. J. clin. Endocrin. 23: 786–791 (1963).
  • BROWN, K. S.; GORDON, B., and CAVONIUS, C. R.: Microphonic potentials from skin predict inner ear defects in cats. Nature, Lond. 228: 1212–1213 (1970).
  • CARHART, R.: Cochlear otosclerosis: audiological considerations. Ann. Otol. Rhinol. Laryng., St. Louis 75: 559–571 (1966).
  • FRASER, G. R.: Profound childhood deafness. J. med. Genet. 1: 118–151 (1964).
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  • JOHNSON, W. J. and HAGAN, P. J.: Hereditary nephropathy and loss of hearing. Arch. Otolaryng. 82: 166–172 (1965).
  • KELEMEN, G. and LINTHICUM, F. H.: Labyrinthine otosclerosis. Acta oto-Iaryng., Stockh. Suppl. 253: 1–68 (1969).
  • KLOTZ, R. E.: Congenital hereditary kidney disease and hearing loss: A case history. Arch. Otolaryng. 69: 560–562 (1959).
  • KON1GSMARK, B. W.; SALMAN, S.; HASKINS, H., and MENGEL, M.: Dominant midfrequency hearing loss. Ann. Otol. Rhinol. Laryng., St. Louis 79: 42–53 (1970).
  • MATKIN, N. D. and CARHART, R.: Auditory profiles associated with Rh incompatibility. Arch. Otolaryng. 84: 502–513 (1966).
  • WILLIAMS, F. and ROBLEE, L. A.: Hereditary nerve deafness. A follow-up of four cases in one family. Arch. Otolaryng. 75: 69–77 (1962).
  • WINTER, L. E.; CRAM, B. M., and BANOVETZ, J. D.: Hearing loss in hereditary renal disease. Arch. Otolaryng. 88: 238–241 (1968).
  • WITKOP, C. J.; NANCE, W. E.; RAWLS, R. F., and WHITE, J. G.: Autosomal recessive oculocutaneous albinism in man: Evidence for genetic heterogeneity. Amer. J. hum. Genet. 22: 55–74 (1970).

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