The study of Lynch syndrome in a special population reveals a strong founder effect and an unusual mutational mechanism in familial adenomatous polyposis. Issue 11 (10th January 2020)

Record Type:: Journal Article
Title:: The study of Lynch syndrome in a special population reveals a strong founder effect and an unusual mutational mechanism in familial adenomatous polyposis. Issue 11 (10th January 2020)
Main Title:: The study of Lynch syndrome in a special population reveals a strong founder effect and an unusual mutational mechanism in familial adenomatous polyposis
Authors:: Siraj, Abdul K
Masoodi, Tariq
Bu, Rong
Parvathareddy, Sandeep Kumar
Siraj, Sarah
Alassiri, Ali
Al-Dayel, Fouad
Alkuraya, Fowzan S
Al-Kuraya, Khawla S
Abstract:
Is Part Of:: Gut. Volume 69:Issue 11(2020)
Journal:: Gut
Issue:: Volume 69:Issue 11(2020)
Issue Display:: Volume 69, Issue 11 (2020)
Year:: 2020
Volume:: 69
Issue:: 11
Issue Sort Value:: 2020-0069-0011-0000
Page Start:: 2048
Page End:: 2049
Publication Date:: 2020-01-10
Subjects:: colorectal cancer -- familial adenomatous polyposis -- HNPCC syndrome
Gastroenterology -- Periodicals
616.33
Journal URLs:: http://gut.bmjjournals.com ↗
http://www.bmj.com/archive ↗
DOI:: 10.1136/gutjnl-2019-320511 ↗
Languages:: English
ISSNs:: 0017-5749
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 17825.xml