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Publikováno v:
South African Journal of Child Health
Background: Waardenburg syndrome (WS) is a rare hereditary disorder essentially characterised by deafness and pigment disorders of the eyes, hair and skin. Method: Between October 2010 and December 2011, we identified six patients with WS during an a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3158::cc7f8f5de2f26cd21f01d030f867de31
https://hdl.handle.net/11427/19694
https://hdl.handle.net/11427/19694
Publikováno v:
South African Journal of Child Health; Feb2014, Vol. 8 Issue 1, p3-5, 3p
