A genetic study of Gardner syndrome and congenital hypertrophy of the retinal pigment epithelium.

Gardner Syndrome (GS) is an autosomal dominant variant of colorectal polyposis with essentially complete penetrance. It is distinguished from the other polyposis syndromes by its delayed age at onset, the number of polyps, and its extracolonic manifestations. The presence of epidermal cysts, bony os...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Lyons, L A, Lewis, R A, Strong, L C, Zuckerbrod, S, Ferrell, R E
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1988
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1715255/
https://ncbi.nlm.nih.gov/pubmed/3422541
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