The clinical phenotype of Lynch syndrome due to germline PMS2 mutations

BACKGROUND AND AIMS: Although the clinical phenotype of Lynch syndrome (also known as Hereditary Nonpolyposis Colorectal Cancer) has been well described, little is known about disease in PMS2 mutation carriers. Now that mutation detection methods can discern mutations in PMS2 from mutations in its p...

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Detalhes bibliográficos
Main Authors: Senter, Leigha, Clendenning, Mark, Sotamaa, Kaisa, Hampel, Heather, Green, Jane, Potter, John D., Lindblom, Annika, Lagerstedt, Kristina, Thibodeau, Stephen N., Lindor, Noralane M., Young, Joanne, Winship, Ingrid, Dowty, James G., White, Darren M., Hopper, John L., Baglietto, Laura, Jenkins, Mark A., de la Chapelle, Albert
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2759321/
https://ncbi.nlm.nih.gov/pubmed/18602922
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1053/j.gastro.2008.04.026
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