Waardenburg’s syndrome a rare entity
Author:
Publisher
Springer Science and Business Media LLC
Subject
Otorhinolaryngology,Surgery
Link
http://link.springer.com/content/pdf/10.1007/BF02996539.pdf
Reference6 articles.
1. Arias S, (1980): Waardenburg’s syndrome - two distinct types. American Journal of Medicine and Genetics 9 : 99 -100.
2. Fisch L, (1959): Deafness as part of an hereditary syndrome. Journal of Laryngolgoy and Otology, 73 : 355 - 382.
3. Marcus RE, (1968): Vestibular function and additional findings in Waardenburg’s syndrome. Acta Otolaryngologica Suppl. (Stockh) 229 : 1 - 30.
4. Rarey KE, Davis LE (1984): Inner ear anomalies in Waardenburg’s syndrome associated with Hirschsprung’s disease. International Journal of Paediatric Otorhinolaryngology, 8 : 181 - 189.
5. Waardenburg PH, (1951): A new syndrome combining developmental anomalies of 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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