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Colon cancer
Citations 1-10 of 102 total displayed.
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Most recent content
(1 Nov 2009):
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Original articles
Mutation prediction models in Lynch syndrome: evaluation in a clinical genetic setting
- D Ramsoekh, M E van Leerdam, A Wagner, E J Kuipers, E W Steyerberg
J. Med. Genet. 2009 46: 745 -751; published online before print as 10.1136/jmg.2009.066589
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Past content
(since Jan 1999):
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Original articles
Comparison of predictive models, clinical criteria and molecular tumour screening for the identification of patients with Lynch syndrome in a population-based cohort of colorectal cancer patients
- J Balmaña, F Balaguer, S Castellví-Bel, E W Steyerberg, M Andreu, X Llor, R Jover, A Castells, S Syngal, for the Gastrointestinal Oncology Group of the Spanish Gastroenterological Association
J. Med. Genet. 2008 45: 557 -563; published online before print as 10.1136/jmg.2008.059311
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Original articles
A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome
- M Clendenning, L Senter, H Hampel, K Lagerstedt Robinson, S Sun, D Buchanan, M D Walsh, M Nilbert, J Green, J Potter, A Lindblom, A de la Chapelle
J. Med. Genet. 2008 45: 340 -345; published online before print as 10.1136/jmg.2007.056150
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Letters to JMG
Direct contact in inviting high-risk members of hereditary colon cancer families to genetic counselling and DNA testing
- K Aktan-Collan, A Haukkala, K Pylvänäinen, H J Järvinen, L A Aaltonen, P Peltomäki, E Rantanen, H Kääriäinen, J-P Mecklin
J. Med. Genet. 2007 44: 732 -738; published online before print as 10.1136/jmg.2007.051581
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Short reports
Biallelic mutation of MSH2 in primary human cells is associated with sensitivity to irradiation and altered RAD51 foci kinetics
- J Barwell, L Pangon, S Hodgson, A Georgiou, I Kesterton, T Slade, M Taylor, S J Payne, H Brinkman, J Smythe, N J Sebire, E Solomon, Z Docherty, R Camplejohn, T Homfray, J R Morris
J. Med. Genet. 2007 44: 516 -520; published online before print as 10.1136/jmg.2006.048660
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Letters to JMG
Pregnancy does not influence colonic polyp multiplicity but may modulate upper gastrointestinal disease in patients with FAP
- Nirosha Suraweera, Andrew Latchford, Amy McCart, Pauline Rogers, Sarah Spain, Oliver Sieber, Robin Phillips, Ian Tomlinson, Andrew Silver
J. Med. Genet. 2007 44: 541 -544; published online before print as 10.1136/jmg.2007.049965
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Letters to JMG
Cancer risks in carriers of the BRCA1/2 Ashkenazi founder mutations
- Luna Kadouri, Ayala Hubert, Yakir Rotenberg, Tamar Hamburger, Michal Sagi, Chovav Nechushtan, Dvorah Abeliovich, Tamar Peretz
J. Med. Genet. 2007 44: 467 -471; published online before print as 10.1136/jmg.2006.048173
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Letters to JMG
Should healthcare providers have a duty to warn family members of individuals with an HNPCC-causing mutation? A survey of patients from the Ontario Familial Colon Cancer Registry
- Kelly Kohut, Michael Manno, Steven Gallinger, Mary Jane Esplen
J. Med. Genet. 2007; 44: 404-407.
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Letters to JMG
Tumour selection advantage of non-dominant negative P53 mutations in homozygotic MDM2-SNP309 colorectal cancer cells
- Hafid Alazzouzi, Gianpaolo Suriano, Angel Guerra, Alberto Plaja, Eloi Espín, Manel Armengol, Pia Alhopuro, Sergia Velho, Yasuhisa Shinomura, Juan José González-Aguilera, Hiroyuki Yamamoto, Lauri A Aaltonen, Víctor Moreno, Gabriel Capellà, Miguel Angel Peinado, Raquel Seruca, Diego Arango, Simó Schwartz, Jr
J. Med. Genet. 2007 44: 75 -80; published online before print as 10.1136/jmg.2006.042572
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Letters to JMG
MDM2 SNP309 accelerates colorectal tumour formation in women
- Gareth L Bond, Chiara Menin, Roberta Bertorelle, Pia Alhopuro, Lauri A Aaltonen, Arnold J Levine
J. Med. Genet. 2006 43: 950 -952; published online before print as 10.1136/jmg.2006.043539
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