about
Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramificationsFamily information service participation increases the rates of mutation testing among members of families with BRCA1/2 mutationsPhenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma-pancreatic carcinoma-prone families: the familial atypical mole melanoma-pancreatic carcinoma syndrome.Diagnosis and management of hereditary colorectal cancer syndromes: Lynch syndrome as a modelCommunication and technology in genetic counseling for familial cancer.Carrier risk status changes resulting from mutation testing in hereditary non-polyposis colorectal cancer and hereditary breast-ovarian cancerPhenotypic and genotypic heterogeneity in the Lynch syndrome: diagnostic, surveillance and management implications.Optimizing the detection of hereditary non-polyposis colorectal cancer: an update.Hereditary cancer syndrome diagnosis: molecular genetic clues and cancer control.Hereditary diffuse gastric cancer: prophylactic surgical oncology implicationsHereditary cancer registries improve the care of patients with a genetic predisposition to cancer: contributions from the Dutch Lynch syndrome registryGenetic counseling for DAPK1 mutation in a chronic lymphocytic leukemia familyHereditary diffuse gastric cancer: diagnosis, genetic counseling, and prophylactic total gastrectomyLynch syndrome-associated extracolonic tumors are rare in two extended families with the same EPCAM deletion.Familial myeloma.Hereditary breast cancer: practical pursuit for clinical translation.Educational and Psychosocial Support Needs in Lynch Syndrome: Implementation and Assessment of an Educational Workshop and Support Group.Anatomical location of urothelial carcinomas of the urinary tract leads to perspectives of specific treatment.The identification and management of hereditary diffuse gastric cancer in a large Jordanian family.Evaluating the utilization of educational materials in communicating about Lynch syndrome to at-risk relatives.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.Accuracy of the routine detection of mutation in mismatch repair genes in patients with susceptibility to hereditary upper urinary tract transitional cell carcinoma
P2860
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P2860
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh-hant
name
Family information service and hereditary cancer.
@en
Family information service and hereditary cancer.
@nl
type
label
Family information service and hereditary cancer.
@en
Family information service and hereditary cancer.
@nl
prefLabel
Family information service and hereditary cancer.
@en
Family information service and hereditary cancer.
@nl
P2860
P1433
P1476
Family information service and hereditary cancer.
@en
P2093
P2860
P304
P356
10.1002/1097-0142(20010215)91:4<625::AID-CNCR1044>3.0.CO;2-4
P407
P577
2001-02-01T00:00:00Z