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Mucosal prolapse in the pathogenesis of Peutz‐Jeghers polyposis

Germline mutations in LKB1 cause the rare cancer prone disorder Peutz‐Jeghers syndrome (PJS). Gastrointestinal hamartomatous polyps constitute the major phenotypic trait in PJS. Hamartomatous polyps arising in PJS patients are generally considered to lack premalignant potential although rare neoplas...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Jansen, M, de Leng, W W J, Baas, A F, Myoshi, H, Mathus‐Vliegen, L, Taketo, M M, Clevers, H, Giardiello, F M, Offerhaus, G J A
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BMJ Group 2006
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC1856361/
https://ncbi.nlm.nih.gov/pubmed/16344569
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/gut.2005.069062
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