MLH1 Ile219Val Polymorphism in Argentinean Families with Suspected Lynch Syndrome

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Bibliographic Details
Published in:	Frontiers in oncology Vol. 6; no. AUG; p. 189
Main Authors:	Dominguez-Valentin, Mev, Wernhoff, Patrik, Cajal, Andrea R, Kalfayan, Pablo G, Piñero, Tamara A, Gonzalez, Maria L, Ferro, Alejandra, Sammartino, Ines, Causada Calo, Natalia S, Vaccaro, Carlos A
Format:	Journal Article
Language:	English
Published:	Switzerland Frontiers Media S.A 24-08-2016
Subjects:	Cancer and Oncology Cancer och onkologi Clinical Medicine I219V Ile219Val Klinisk medicin Lynch Syndrome Medical and Health Sciences Medicin och hälsovetenskap MLH1 MSH2 Mutation Oncology mutation MSH2 MLH1 Ile219Val Lynch syndrome
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Bibliography:	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Rupert Langer, University of Bern, Switzerland Reviewed by: Gisela Keller, Technische Universität München, Germany; Elgin Ozkan, Ankara University Medical School, Turkey; Angel Lanas, University of Zaragoza, Spain Specialty section: This article was submitted to Gastrointestinal Cancers, a section of the journal Frontiers in Oncology
ISSN:	2234-943X 2234-943X
DOI:	10.3389/fonc.2016.00189