| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Kenneth Offit | Q20732365 |
| P2093 | author name string | Khedoudja Nafa | |
| Nathan A Ellis | |||
| Harvey G Moore | |||
| Jose G Guillem | |||
| Arnold J Markowitz | |||
| Emily Glogowski | |||
| Rob Finch | |||
| Crystal Palmer | |||
| P2860 | cites work | Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC. | Q54559294 |
| A636P is associated with early-onset colon cancer in Ashkenazi Jews. | Q54788578 | ||
| Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease | Q57567959 | ||
| A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: Meeting Highlights and Bethesda Guidelines | Q57978042 | ||
| Clinical Findings with Implications for Genetic Testing in Families with Clustering of Colorectal Cancer | Q58006261 | ||
| Clustering of colorectal cancer in families of probands under 40 years of age | Q71513218 | ||
| Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer | Q28253384 | ||
| The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer | Q28256988 | ||
| Gastrointestinal polyposis syndromes | Q33599177 | ||
| Clinical implications of genetic testing of hereditary nonpolyposis colorectal cancer | Q33764554 | ||
| Genetic anthropology of the colorectal cancer-susceptibility allele APC I1307K: evidence of genetic drift within the Ashkenazim | Q33905286 | ||
| MSH2 c.1452-1455delAATG is a founder mutation and an important cause of hereditary nonpolyposis colorectal cancer in the southern Chinese population | Q33909800 | ||
| The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population | Q34161196 | ||
| Recurrent germline mutation in MSH2 arises frequently de novo | Q35435822 | ||
| Genetic instability occurs in the majority of young patients with colorectal cancer | Q38297232 | ||
| Phenotypic analysis of hMSH2 mutations in mouse cells carrying human chromosomes. | Q40770785 | ||
| Age and origin of two common MLH1 mutations predisposing to hereditary colon cancer | Q42011353 | ||
| Multiple HNPCC tumours: ask the family! | Q43087314 | ||
| A missense mutation in both hMSH2 and APC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening | Q43199969 | ||
| Population-based molecular detection of hereditary nonpolyposis colorectal cancer | Q43783854 | ||
| A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States | Q46655105 | ||
| Germ-line mutation of the hMSH6/GTBP gene in an atypical hereditary nonpolyposis colorectal cancer kindred | Q48044118 | ||
| Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer | Q48084125 | ||
| Hereditary susceptibility to colorectal cancer. Relatives of early onset cases are particularly at risk. | Q52869239 | ||
| P433 | issue | 3-4 | |
| P304 | page(s) | 223-227 | |
| P577 | publication date | 2004-01-01 | |
| P1433 | published in | Familial Cancer | Q15761917 |
| P1476 | title | A636P testing in Ashkenazi Jews | |
| P478 | volume | 3 |
| Q44095031 | A novel MSH2 germline mutation in a Druze HNPCC family |
| Q36808349 | High risk of colorectal and endometrial cancer in Ashkenazi families with the MSH2 A636P founder mutation |
| Q55465499 | Homozygosity of MSH2 c.1906G-->C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type I. |
| Q51889166 | Mutation spectrum in HNPCC in the Israeli population. |
Search more.