Keratoderma hereditarium mutilans (Vohwinkel's syndrome) associated with congenital deaf-mutism
- 29 July 2006
- journal article
- case report
- Published by Wiley in British Journal of Dermatology
- Vol. 132 (4) , 617-620
- https://doi.org/10.1111/j.1365-2133.1995.tb08721.x
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
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