Who should be sent for genetic testing in hereditary colorectal cancer syndromes?
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Potential of apoptotic pathway-targeted cancer therapeutic research: Where do we stand?Importance of age of onset in pancreatic cancer kindredsUtility of p16 immunohistochemistry for the identification of Lynch syndromeModel-based prediction of defective DNA mismatch repair using clinicopathological variables in sporadic colon cancer patients.Mismatch repair protein expression and colorectal cancer in Hispanics from Puerto RicoUnderdiagnosis of Lynch syndrome involves more than family history criteriaMaking sense of missense in Lynch syndrome: the clinical perspectiveLynch syndrome: an updated reviewLung cancer therapeutics that target signaling pathways: an update.Diagnosis and management of hereditary colorectal cancer syndromes: Lynch syndrome as a modelOn the TRAIL to successful cancer therapy? Predicting and counteracting resistance against TRAIL-based therapeutics.Comparison of the clinical prediction model PREMM(1,2,6) and molecular testing for the systematic identification of Lynch syndrome in colorectal cancer.Erlotinib in non-small-cell lung cancer.Genetic counseling for DAPK1 mutation in a chronic lymphocytic leukemia familyClinical implications of microsatellite instability in sporadic colon cancersColorectal cancer cases and relatives of cases indicate similar willingness to receive and disclose genetic information.Evaluating women with ovarian cancer for BRCA1 and BRCA2 mutations: missed opportunities.Combined modality therapy with TRAIL or agonistic death receptor antibodies.The therapeutic potential of TRAIL receptor signalling in cancer cells.Hereditary breast cancer: practical pursuit for clinical translation.Lynch syndrome diagnostics: decision-making process for germ-line testing.Genetics, biomarkers, hereditary cancer syndrome diagnosis, heterogeneity and treatment: a review.Mismatch repair analysis of inherited MSH2 and/or MSH6 variation pairs found in cancer patients.Synchronous rectal and gastric cancer in a fighter pilot: aeromedical concerns.Assessing pathogenicity: overview of results from the IARC Unclassified Genetic Variants Working Group.Hereditary non-polyposis colorectal cancer/Lynch syndrome in Korean patients with endometrial cancer.Anatomical location of urothelial carcinomas of the urinary tract leads to perspectives of specific treatment.A proportion of hereditary upper urinary tract urothelial carcinomas are misclassified as sporadic according to a multi-institutional database analysis: proposal of patient-specific risk identification tool.
P2860
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P2860
Who should be sent for genetic testing in hereditary colorectal cancer syndromes?
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Who should be sent for genetic testing in hereditary colorectal cancer syndromes?
@en
type
label
Who should be sent for genetic testing in hereditary colorectal cancer syndromes?
@en
prefLabel
Who should be sent for genetic testing in hereditary colorectal cancer syndromes?
@en
P2093
P356
P1476
Who should be sent for genetic testing in hereditary colorectal cancer syndromes?
@en
P2093
C Richard Boland
Henry T Lynch
Jane F Lynch
Miguel A Rodriguez-Bigas
Patrick M Lynch
P304
P356
10.1200/JCO.2006.10.3119
P407
P577
2007-08-01T00:00:00Z