International Journal of Pediatric Otorhinolaryngology
Volume 59, Issue 2 , Pages 137-141 , 14 June 2001

Temporal bone histopathology in trisomy 22

Received 23 December 2000 ,Accepted 24 February 2001.

References 

  1. Hsu LYF, Shapiro LR, Gertner M, Lieber E, Hirschhorn K. Trisomy 22: a clinical entity. J. Pediatr. 1971;79:12–19
  2. Kadotani T, Katano T, Yamaoka H, Murakami M, Nakamoto Y, Watanabe Y. Clinical and cytogenetic features of a case with trisomy 22. Proc. Jpn. Acad. 1978;54B:163–166
  3. Crowe CA, Schwartz S, Black CJ, Jaswaney V. Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes. Am. J. Med. Genet. 1997;71:406–413
  4. Arnold W, Schuknecht HF, von Voss H. Felsenbeinbefunde beider Trisomy 22. Laryng. Rhinol. 1981;60:545–549
  5. Kadotani T, Katano T, Yamaoka H, Watanabe Y. A case of partial trisomy 22 without cat-eye stigmata. Proc. Jpn. Acad. 1978;54B:217–221
  6. Katano T, Yamaoka H, Takiguchi T, Kadotani T. Auditory disturbance due to trisomy 22. Lancet. 1979;1:276–277

PII: S0165-5876(01)00459-1

International Journal of Pediatric Otorhinolaryngology
Volume 59, Issue 2 , Pages 137-141 , 14 June 2001

Article Tools

* Image Usage & Resolution