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Comprehensive molecular analysis of mismatch repair gene defects in suspected Lynch Syndrome (Hereditary Non-polyposis Colorectal Cancer) cases

An accurate algorithm is essential for effective molecular diagnosis of hereditary colorectal cancer. Here we have extended the analysis of 71 colorectal cancer cases suspected to be Lynch Syndrome cases for MSH2, MLH1, MSH6 and PMS2 gene defects. All cases were screened for mutations in MSH2, MLH1...

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Bibliografiset tiedot
Päätekijät: Mueller, James, Gazzoli, Isabella, Bandipalliam, Prathap, Garber, Judy E., Syngal, Sapna, Kolodner, Richard D.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2009
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2761236/
https://ncbi.nlm.nih.gov/pubmed/19690142
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1158/0008-5472.CAN-09-0358
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