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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Detaylı Bibliyografya
Asıl Yazarlar: Entius, M, Westerman, A, Giardiello, F, van Velthuysen, M-L F, Polak, M, Slebos, R, Wilson, J, Hamilton, S, Offerhaus, G
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1997
Konular:
Cancer
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1891488/
https://ncbi.nlm.nih.gov/pubmed/9378385
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