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Cochlear Implants International
An Interdisciplinary Journal for Implantable Hearing Devices
Volume 5, 2004 - Issue sup1
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Case Reports

Cochlear implantation in a case with Waardenburg syndrome

Pages 212-214 | Published online: 13 Dec 2013

REFERENCES

  • Lalwani A, Baldwin C, Morell R, Friedman T, San Agustin T, Milunsky A et al. (1994) A locus for Waardenburg syndrome type II maps to chromosome 1p13.3-2.1. American Journal of Human Genetics 55(Suppl): A14.
  • Nakashima S, Sando I, Takahashi H, Hashida Y (1992) Temporal bone histopathologic findings of Waardenburg's syndrome: a case report. Laryngoscope 102(5): 563–567.
  • Oysu C, Oysu A, Aslan I, Tinaz M (2001) Temporal bone imaging findings in Waardenburg's syndrome. International Journal of Pediatric Otorhinolaryngology 58(3): 215–221.
  • Selicomi A, Guemeri S, Ratti A, Pizzuti A (2002) Cytogenetic mapping of a novel locus for type II Waardenburg syndrome. Human Genetics 110(1): 64–67.
  • Sugii A, Iwaki T, Doi K, Takahashi Y, Yamamoto K, Fuse Y et al. (2000) Cochlear implant in a young child with Waardenburg syndrome. Advances in Otorhinolaryngology 57:215–219.
  • Tassabehji M, Newton VE, Liu XZ, Brady A, Donnai D, Krajewska-Walasek M et al. (1995) The mutational spectrum in Waardenburg syndrome. Human Molecular Genetics 4(11): 2131–2137.
  • Waardenburg P (1951) A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair with congenital deafness. American Journal of Human Genetics 3: 195–253.

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