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Original Article

Population-Based Genetic Study of Childhood Hearing Impairment in the Trent Region of the United Kingdom: Estudio Genetico Sobre Sordera Infantil en una Poblacion de la Region de Trent en el Reino Unido

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Pages 226-231 | Received 15 Apr 2000, Accepted 25 Jun 2000, Published online: 07 Jul 2009

References

  • Davis A, Parving A. Towards appropriate epidemiological data on childhood hearing disability: a comparative European study of birth cohorts 1982-88. J Audiol Med 1994; 3(1)35–47
  • Reardon W. Genetic deafness. J Med Genet 1992; 29: 521–526
  • Morton N E. Genetic epidemiology of hearing impairment. Ann N Y Acad Sci 1991; 630: 16–31
  • Van Camp G, Smith R JH. Hereditary hearing loss homepage, http://dnalab-www.uia.ac.be/dnalab/hhh/
  • Zelante L, Gasparini P, Estivill X, et al. Connexin-26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans. Hum Mol Genet 1997; 6: 1605–1609
  • Denoyelle F, Weil D, Maw M A, et al. Prelingual deafness: high prevalence of a 30delG mutation in the Connexin 26 gene. Hum Mol Genet 1997; 6: 2173–2177
  • Estivill X, Fortina P, Surrey S, et al. Connexin-26 mutations in sporadic and inherited sensorineural deafness. Lancet 1998; 351: 394–398
  • Denoyelle F, Marlin S, Weil D, et al. Clinical features of the prevalent form of childhood deafness, DFNB1, to a Connexin-26 gene defect: implications for genetic counselling. Lancet 1999; 353: 1298–1303
  • Mueller R F, Nehammer A, Middleton A, et al. Congenital non-syndromal sensorineural hearing impairment due to Connexin 26 gene mutations–molecular and audiological findings. Int J Pediatr Otolaryngol 1999; 50: 3–13
  • Fortnum H M, Davis A C. Epidemiology of permanent childhood hearing impairment in Trent Region, 1985–1993. Br J Audiol 1997; 31: 409–446
  • Parker M J, Fortnum H, Young I D, Davis A C. Genetics and deafness: what do families want?. J Med Genet. in press
  • Storm K, Willcox S, Flothman K, Van Camp G. Determination of the carrier frequency of the common GJB2 (Connexin-26) 35delG mutation in the Belgian population using an easy and reliable screening method. Hum Mutat 1999; 14: 263–266
  • Tookey P A, Peckham C S. Surveillance of congenital rubella in Great Britain, 1971-96. BMJ 1999; 318: 769–770
  • Armitage I M, Burke J P, Buffin J T. Visual impairment in severe and profound sensorineural deafness. Arch Dis Child 1995; 73(1)53–56
  • Parker M J, Fortnum H, Young I D, Davis A C. Variations in genetic assessment and recurrence risks quoted for childhood deafness: a survey of clinical geneticists. J Med Genet 1999; 36: 125–130

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