Universal dyschromatosis, small stature and high-tone deafness
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2230.1977.tb01536.x/fullpdf
Reference15 articles.
1. A FAMILIAL PIGMENTARY ANOMALY
2. Dyskeratosis Congenita and Familial Pancytopenia
3. Erythema Dyschromicum Perstans
4. UNIVERSAL DYSCHROMATOSIS
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