138 related articles for article (PubMed ID: 11494233)
101. The case for surveillance of high-risk' families.
Dunlop MG
Eur J Gastroenterol Hepatol; 1998 Mar; 10(3):229-33. PubMed ID: 9585026
[TBL] [Abstract][Full Text] [Related]
102. Multiple tumors and a novel E2F-4 mutation. A case report.
Matsubara N; Yoshitaka T; Matsuno T; Ikeda M; Isozaki H; Tanaka N; Shimizu K
Digestion; 2000; 62(2-3):213-6. PubMed ID: 11025371
[TBL] [Abstract][Full Text] [Related]
103. Association between Aurora-A kinase polymorphisms and age of onset of hereditary nonpolyposis colorectal cancer in a Caucasian population.
Chen J; Sen S; Amos CI; Wei C; Jones JS; Lynch P; Frazier ML
Mol Carcinog; 2007 Apr; 46(4):249-56. PubMed ID: 17219423
[TBL] [Abstract][Full Text] [Related]
104. Broadening risk profile in familial colorectal cancer type X; increased risk for five cancer types in the national Danish cohort.
Therkildsen C; Rasmussen M; Smith-Hansen L; Kallemose T; Lindberg LJ; Nilbert M
BMC Cancer; 2020 Apr; 20(1):345. PubMed ID: 32321466
[TBL] [Abstract][Full Text] [Related]
105. Familial Colorectal Cancer Type X.
Zetner DB; Bisgaard ML
Curr Genomics; 2017 Aug; 18(4):341-359. PubMed ID: 29081690
[TBL] [Abstract][Full Text] [Related]
106. Distinct gene expression signatures in lynch syndrome and familial colorectal cancer type x.
Dominguez-Valentin M; Therkildsen C; Veerla S; Jönsson M; Bernstein I; Borg A; Nilbert M
PLoS One; 2013; 8(8):e71755. PubMed ID: 23951239
[TBL] [Abstract][Full Text] [Related]
107. Familial colorectal cancer: eleven years of data from a registry program in Switzerland.
Kovac M; Laczko E; Haider R; Jiricny J; Mueller H; Heinimann K; Marra G
Fam Cancer; 2011 Sep; 10(3):605-16. PubMed ID: 21671081
[TBL] [Abstract][Full Text] [Related]
108. Genomic instability and carcinogenesis: an update.
Abdel-Rahman WM
Curr Genomics; 2008 Dec; 9(8):535-41. PubMed ID: 19516960
[TBL] [Abstract][Full Text] [Related]
109. Correlations between phenotype and microsatellite instability in HNPCC: implications for genetic testing.
Palmirotta R; Matera S; Curia MC; Aceto G; el Zhobi B; Verginelli F; Guadagni F; Casale V; Stigliano V; Messerini L; Mariani-Costantini R; Battista P; Cama A
Fam Cancer; 2004; 3(2):117-21. PubMed ID: 15340262
[TBL] [Abstract][Full Text] [Related]
110. Aetiology of colorectal cancer and relevance of monogenic inheritance.
Ponz de Leon M; Benatti P; Borghi F; Pedroni M; Scarselli A; Di Gregorio C; Losi L; Viel A; Genuardi M; Abbati G; Rossi G; Menigatti M; Lamberti I; Ponti G; Roncucci L
Gut; 2004 Jan; 53(1):115-22. PubMed ID: 14684585
[TBL] [Abstract][Full Text] [Related]
111. Rapidly progressive adenomatous polyposis in a patient with germline mutations in both the APC and MLH1 genes: the worst of two worlds.
Scheenstra R; Rijcken FE; Koornstra JJ; Hollema H; Fodde R; Menko FH; Sijmons RH; Bijleveld CM; Kleibeuker JH
Gut; 2003 Jun; 52(6):898-9. PubMed ID: 12740349
[TBL] [Abstract][Full Text] [Related]
112. The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas.
Cunningham JM; Kim CY; Christensen ER; Tester DJ; Parc Y; Burgart LJ; Halling KC; McDonnell SK; Schaid DJ; Walsh Vockley C; Kubly V; Nelson H; Michels VV; Thibodeau SN
Am J Hum Genet; 2001 Oct; 69(4):780-90. PubMed ID: 11524701
[TBL] [Abstract][Full Text] [Related]
113. Hereditary nonpolyposis colorectal cancer (Lynch syndrome): criteria for identification and management.
Kouraklis G; Misiakos EP
Dig Dis Sci; 2005 Feb; 50(2):336-44. PubMed ID: 15745097
[TBL] [Abstract][Full Text] [Related]
114. Molecular basis of HNPCC: mutations of MMR genes.
Papadopoulos N; Lindblom A
Hum Mutat; 1997; 10(2):89-99. PubMed ID: 9259192
[TBL] [Abstract][Full Text] [Related]
115. Clinical and biologic heterogeneity of hereditary nonpolyposis colorectal cancer.
Benatti P; Roncucci L; Ganazzi D; Percesepe A; Di Gregorio C; Pedroni M; Borghi F; Sala E; Scarselli A; Menigatti M; Rossi G; Genuardi M; Viel A; Ponz De Leon M
Int J Cancer; 2001 Sep; 95(5):323-8. PubMed ID: 11494233
[TBL] [Abstract][Full Text] [Related]
116. Extended microsatellite analysis in microsatellite stable, MSH2 and MLH1 mutation-negative HNPCC patients: genetic reclassification and correlation with clinical features.
Schiemann U; Müller-Koch Y; Gross M; Daum J; Lohse P; Baretton G; Muders M; Mussack T; Kopp R; Holinski-Feder E
Digestion; 2004; 69(3):166-76. PubMed ID: 15118395
[TBL] [Abstract][Full Text] [Related]
117. Clinical features and mismatch repair gene mutation screening in Chinese patients with hereditary nonpolyposis colorectal carcinoma.
Liu SR; Zhao B; Wang ZJ; Wan YL; Huang YT
World J Gastroenterol; 2004 Sep; 10(18):2647-51. PubMed ID: 15309712
[TBL] [Abstract][Full Text] [Related]
118.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
119.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
120.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]