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Peutz-Jeghers polyps, dysplasia, and K-ras codon 12 mutations
Background—Peutz-Jeghers syndrome (PJS) is a rare, autosomal dominant, polyposis syndrome, associated with an increased risk of gastrointestinal and extragastrointestinal malignancy. Occasionally dysplasia occurs in PJS polyps. Aims—In colorectal carcinomas, mutations in codon 12 of the K-ras oncog...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
1997
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1891488/ https://ncbi.nlm.nih.gov/pubmed/9378385 |
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