Congenital muscular dystrophy and epidermolysis bullosa simplex

The Journal of Pediatrics

Volumn 114, Issue 1, 1989, Pages 104-107

  Kletter, Gad ^a   Evans, Owen B ^a   Lee, James Anthony ^a   Melvin, Barbara ^a   Yates, Anne Bridges ^a   Bock, Hans Georg Otto ^a  

^a UNIVERSITY OF MISSISSIPPI MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; DISEASE ASSOCIATION; EPIDERMOLYSIS BULLOSA; FAMILY HISTORY; HEREDITY; HUMAN; MUSCULAR DYSTROPHY; PEDIGREE; PRIORITY JOURNAL; ULTRASTRUCTURE;

EPIDERMOLYSIS BULLOSA; FEMALE; HUMAN; INFANT, NEWBORN; MALE; MUSCULAR DYSTROPHIES; PEDIGREE;

EID: 0024509171     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(89)80614-6     Document Type: Article

References (8)

1. Epidermolysis bullosa: clinical aspects, pathology and recent advances in research
2. Hereditary epidermolysis bullosa
3. Congenital muscular dystrophy: a clinicopathologic report of 24 cases
4. Fukuyama-type congenital muscular dystrophy
5. Congenital muscular dystrophy with cerebral white matter spongiosis
6. Monoclonal IgM antibody precipitating with chondroitin sulfate C from patients with axonal polyneuropathy and epidermolysis
7. Het voorkomen van epidermolysis bullosa hereditaria dystrophica en progressieve spierdystrofie in een gezin
8. Epidermolysis bullosa simplex associated with muscular dystrophy with recessive inheritance