Prenatal diagnosis for recessive dystrophic epidermolysis bullosa in 10 families by mutation and haplotype analysis in the type VII collagen gene (COL7A1)

Molecular Medicine

Volumn 2, Issue 1, 1996, Pages 59-76

  Christiano, Angela M ^a   LaForgia, Sal ^a   Paller, Amy S ^b   McGuire, Joseph ^c   Shimizu, Hiroshi ^d   Uitto, Jouni ^a  

^a THOMAS JEFFERSON UNIVERSITY   (United States)

^b NORTHWESTERN UNIVERSITY   (United States)

^c STANFORD UNIVERSITY MEDICAL CENTER   (United States)

^d KEIO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

COLLAGEN TYPE 7; DNA;

AMNIOCENTESIS; ARTICLE; BASEMENT MEMBRANE; CHORION VILLUS SAMPLING; CHROMOSOME 3P; CLINICAL ARTICLE; DERMOEPIDERMAL JUNCTION; EPIDERMOLYSIS BULLOSA DYSTROPHICA; FAMILY; FEMALE; FETUS; GENE MUTATION; HAPLOTYPE; HETEROZYGOTE; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RECESSIVE INHERITANCE; SKIN BIOPSY;

EID: 0029669182     PISSN: 10761551     EISSN: None     Source Type: Journal    
DOI: 10.1007/bf03402203     Document Type: Article

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