Linkage analysis in familial non-Lynch syndrome colorectal cancer families from Sweden.
Ontology highlight
ABSTRACT: Family history is a major risk factor for colorectal cancer and many families segregate the disease as a seemingly monogenic trait. A minority of familial colorectal cancer could be explained by known monogenic genes and genetic loci. Familial polyposis and Lynch syndrome are two syndromes where the predisposing genes are known but numerous families have been tested without finding the predisposing gene. We performed a genome wide linkage analysis in 121 colorectal families with an increased risk of colorectal cancer. The families were ascertained from the department of clinical genetics at the Karolinska University Hospital in Stockholm, Sweden and were considered negative for Familial Polyposis and Lynch syndrome. In total 600 subjects were genotyped using single nucleotide polymorphism
SUBMITTER: Kontham V
PROVIDER: S-EPMC3859667 | biostudies-literature | 2013
REPOSITORIES: biostudies-literature
ACCESS DATA