RHBDF2 mutations are associated with tylosis, a familial esophageal cancer syndrome

Blaydon, Diana C. and Etheridge, Sarah L. and Risk, Janet M. and Hennies, Hans-Christian and Gay, Laura J. and Carroll, Rebecca and Plagnol, Vincent and McRonald, Fiona E. and Stevens, Howard P. and Spurr, Nigel K. and Bishop, D.Timothy and Ellis, Anthony and Jankowski, Janusz and Field, John K. and Leigh, Irene M. and South, Andrew P. and Kelsell, David P. (2012) RHBDF2 mutations are associated with tylosis, a familial esophageal cancer syndrome. American Journal of Human Genetics, 90 (2). pp. 340-346. ISSN 1537-6605 (Online); 0002-9297 (Print)

Full text not available from this repository.
Item Type: Article
Additional Information: Published online 19 January 2012. Issue date: 10 February 2012.
Subjects: R Medicine > RC Internal medicine > RC0254 Neoplasms. Tumors. Oncology (including Cancer)
Divisions: ?? cancer ??
Depositing User: Users 7076 not found.
Date Deposited: 09 Mar 2012 16:37
Last Modified: 09 Oct 2014 12:04
URI: http://repository.liv.ac.uk/id/eprint/5455

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