Improving the uptake of predictive testing and colorectal screening in Lynch syndrome: a regional primary care survey-Reference-Cited by-同舟云学术

Improving the uptake of predictive testing and colorectal screening in Lynch syndrome: a regional primary care survey

Published:2015-02-04 Issue:6 Volume:87 Page:517-524
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Barrow P.¹,Green K.²,Clancy T.²³,Lalloo F.²³,Hill J.¹,Evans D.G.²³

Affiliation:

1. Department of Colorectal Surgery, Manchester Royal Infirmary; Manchester UK

2. Manchester Centre for Genomic Medicine; Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Sciences Centre (MAHSC); Manchester UK

3. Manchester Centre for Genomic Medicine, Institute of Human Development, Faculty of Medical and Human Sciences; University of Manchester, MAHSC; Manchester UK

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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2. Review of the Lynch Syndrome: history, molecular genetics, screening, differential diagnosis and medicolegal ramifications;Lynch;Clin Genet,2009

3. Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer);Vasen;J Medical Genet,2007

4. Guidelines for colorectal cancer screening and surveillance in moderate and high risk groups (update from 2002);Cairns;Gut,2010

5. Colorectal cancer in HNPCC: cumulative lifetime incidence, survival and tumour distribution. A report of 121 families with proven mutations;Barrow;Clin Genet,2008

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