Junctional epidermolysis bullosa: Diagnosis and management of a patient with the Herlitz variant
Author:
Publisher
Elsevier BV
Subject
General Medicine,Pediatrics, Perinatology and Child Health,Surgery
Reference14 articles.
1. Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa;Fine;J Am Acad Dermatol,1991
2. The generalized atrophic benign form of junctional epidermolysis bullosa;Paller;Arch Dermatol,1986
3. Epidermolysis bullosa hereditaria letalis;Pearson;Arch Dermatol,1974
4. Identification of a homozygous one-basepair deletion in exon 14 of the LAMB3 gene in a patient with Herlitz junctional epidermolysis bullosa and prenatal diagnosis in a family at risk for recurrence;Vailly;J Invest Dermatol,1995
5. Cloning of the laminin α3 chain gene (LAMA3) and identification of a homozygous deletion in a patient with Herlitz junctional epidermolysis bullosa;Vidal;Genomics,1995
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