학술논문
MSH2 genomic deletions are a frequent cause of HNPCC.
Document Type
Article
Author
Source
Subject
*GENETICS of colon cancer
*GENOMICS
*
Language
ISSN
1061-4036
Abstract
Studies the association of MSH2 genomic deletions with hereditary non-polyposis colorectal cancer in Amsterdam, Netherlands. Prevalence of MSH2 mutations in patients with the disorder; Restriction patterns indicative of genomic deletions in MSH2.