Disease: Epidermolysis bullosa dystrophica- Bart type
- A Case Report of an Infant with Autosomal Recessive Dystrophic Epidermolysis Bullosa: COL7A1 Gene Mutations at C2005T and G7922A
- Aplasia cutis congenita with dystrophic epidermolysis bullosa: Bart syndrome
- Autosomal dominant epidermolysis bullosa dystrophica: are the Cockayne-Touraine, the Pasini and the Bart-types different expressions of the same mutant gene?
- Bart's syndrome in a family affected three consecutive generations with mutation c.6007G>A in COL7A1
- Bart's syndrome in a family affected three consecutive generations with mutation c.6007G>A in COL7A1
- Bart's Syndrome with Novel Frameshift Mutations in the COL7A1 Gene
- Bart's syndrome. Ultrastructure and genetic linkage
- Clinical phenotype of Bart's syndrome seen in a family with dominant dystrophic epidermolysis bullosa
- Congenital scalp defects with distal limb anomalies (Adams-Oliver syndrome): report of ten cases and review of the literature
- Genetic basis of Bart's syndrome: a glycine substitution mutation in the type VII collagen gene
- Genetic basis of Bart's syndrome: a glycine substitution mutation in type VII collagen gene
- Genetic linkage between the collagen VII (COL7A1) gene and the autosomal dominant form of dystrophic epidermolysis bullosa in two Dutch kindreds
- Genotype-phenotype correlations on epidermolysis bullosa with congenital absence of skin: A comprehensive review
- Hereditary epidermolysis bullosa. Epidemiology and clinical classification of 23 cases
- Novel glycine substitution mutations in COL7A1 reveal that the Pasini and Cockayne-Touraine variants of dominant dystrophic epidermolysis bullosa are allelic
- Recessive dystrophic epidermolysis bullosa: presentation of two forms