Síndrome de Bart asociado a epidermólisis ampollosa hereditaria letal (Herlitz)
Author:
Publisher
Elsevier BV
Subject
Dermatology,Histology,Pathology and Forensic Medicine
Reference17 articles.
1. Congenital localized absence of skin and associated abnormalities resembling epidermolysis bullosa. A new syndrome;Bart;Arch Dermatol,1966
2. Dystrophic epidermolysis bullosa presenting with congenital localized absence of skin: report of four cases;Wojnarowska;Br J Dermatol,1983
3. Bart's syndrome: microscopic, ultrastructural, and immunofluorescent mapping features;Butler;Pediatr Dermatol,1986
4. Clinical phenotype of Bart's syndrome seen in a family with dominant dystrophic epidermolysis bullosa;Wakasugi;J Dermatol,1998
5. Bart's syndrome. Ultrastructure and genetic linkage;Zelickson;Arch Dermatol,1995
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