Marie Unna Hypotrichosis in a Chinese Family
Author:
Affiliation:
1. National Skin Centre and
2. Department of Pathology, National University of Singapore, Singapore
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology and Child Health
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1525-1470.2002.00070.x
Reference14 articles.
1. Uber hypotrichosis congenita hereditaria;Unna M;Derm Wschr,1925
2. Hypotrichosis congenita hereditaria type M;Ludwig E;Unna Arch Derm Syph,1953
3. Hypotrichosis congenita hereditaria Marie Unna;Borelli S;Hautarzt,1954
4. Marie Unna Congenital Hypotrichosis: Clinical Description, Histopathology, Scanning Electron Microscopy of a Previously Unreported Large Pedigree
5. Marie‐Unna hereditary hypotrichosis;Argenziano G;Eur J Dermatol,1999
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1. Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report;Journal of the American Academy of Dermatology;2011-04
2. Marie-Unna Hereditary Hypotrichosis: Case Report and Review of the Literature;Pediatric Dermatology;2011-03
3. Disorders of Hair and Nails;Hurwitz Clinical Pediatric Dermatology;2011
4. Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a U2HR mutation;American Journal of Medical Genetics Part A;2010-09-02
5. Diseases of cutaneous appendages;Weedon's Skin Pathology;2010
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