Hereditary nonpolyposis colorectal cancer
Autosomal dominant genetic condition associated with a high risk of cancer in the colon
Ratings
0
Nobody has rated this yet. Be the first!
Subject of
11
Novel germline MSH2 mutation in lynch syndrome patient surviving multiple cancers
Characterization of New Founder Alu-Mediated Rearrangements in MSH2 Gene Associated with a Lynch Syndrome Phenotype
Molecular Analysis of Familial Endometrial Carcinoma: A Manifestation of Hereditary Nonpolyposis Colorectal Cancer or a Separate Syndrome?
Computational and cellular studies reveal structural destabilization and degradation of MLH1 variants in Lynch syndrome
Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes
Survival from colorectal carcinoma in HNPCC families as compared to the general population in Lithuania--initial results
The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumours
Splicing analysis for exonic and intronic mismatch repair gene variants associated with Lynch syndrome confirms high concordance between minigene assays and patient RNA analyses
Cancer Risks for PMS2-Associated Lynch Syndrome
Surveillance for endometrial cancer in hereditary nonpolyposis colorectal cancer syndrome
