Cowden disease: gene marker studies and measurements of epidermal growth factor.

Cowden disease (CD) is a familial syndrome characterized by tumors of the skin, oral mucosa, breast, thyroid, and intestinal epithelium. Since the syndrome is inherited as an autosomal dominant, we examined a battery of gene markers in a family with CD to detect linkage between the CD gene and known...

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Detalles Bibliográficos
Main Authors: Carlson, H E, Burns, T W, Davenport, S L, Luger, A M, Spence, M A, Sparkes, R S, Orth, D N
Formato: Artigo
Idioma:Inglês
Publicado: 1986
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Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC1684853/
https://ncbi.nlm.nih.gov/pubmed/3487976
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