Single-amplicon MSH2 A636P Mutation Testing in Ashkenazi Jewish Patients With Colorectal Cancer: Role in Presurgical Management

OBJECTIVE: This study summarizes our initial experience with prospective, single-amplicon (mutation-specific) A636P testing in Ashkenazi Jewish patients at risk for Hereditary Nonpolyposis Colorectal Cancer (HNPCC). SUMMARY BACKGROUND DATA: We previously described a founder mutation, MSH2*1906G >...

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Detalhes bibliográficos
Main Authors: Guillem, Jose G., Glogowski, Emily, Moore, Harvey G., Nafa, Khedoudja, Markowitz, Arnold J., Shia, Jinru, Offit, Kenneth, Ellis, Nathan A.
Formato: Artigo
Idioma:Inglês
Publicado em: 2007
Assuntos:
Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1877028/
https://ncbi.nlm.nih.gov/pubmed/17414604
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/01.sla.0000252589.26244.d4
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