Homozygosity for a CHEK2 I100deIC mutation identified in familial colorectal cancer does not lead to a severe clinical phenotype

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Bibliographic Details
Published inThe Journal of pathology Vol. 206; no. 2; pp. 198 - 204
Main Authors VAN PUIJENBR-OEK, Marjo, VAN ASPEREN, Christ J, VAN MIL, Anneke, DEVILEE, Peter, VAN WEZEL, Tom, MORREAU, Hans
Format Journal Article
LanguageEnglish
Published Chichester Wiley 2005
Subjects
Biological and medical sciences
Gastroenterology. Liver. Pancreas. Abdomen
Investigative techniques, diagnostic techniques (general aspects)
Medical sciences
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Stomach. Duodenum. Small intestine. Colon. Rectum. Anus
Tumors
Rectal disease
Colorectal cancer
TMA
Malignant tumor
Homozygosity
Colonic disease
HNPCC
Anatomic pathology
Phenotype
Tissue microarrays
CHEK2
Digestive diseases
Intestinal disease
Familial cancer
Genetics
Mutation
Severe
Mechanism of action
familial colorectal cancer
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ISSN:0022-3417
1096-9896