A germline missense mutation in exon 3 of the MSH2 gene in a Lynch syndrome family: correlation with phenotype and localization assay-Reference-Cited by-同舟云学术

A germline missense mutation in exon 3 of the MSH2 gene in a Lynch syndrome family: correlation with phenotype and localization assay

Published:2017-08-07 Issue:2 Volume:17 Page:215-224
ISSN:1389-9600
Container-title:Familial Cancer
language:en
Short-container-title:Familial Cancer

Author:

Bianchi Francesca,Maccaroni Elena^ORCID,Belvederesi Laura,Brugiati Cristiana,Giampieri Riccardo,Bini Federica,Bracci Raffaella,Pagliaretta Silvia,Del Prete Michela,Piva Francesco,Mandolesi Alessandra,Scarpelli Marina,Berardi Rossana

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics (clinical),Oncology,Genetics

Link

http://link.springer.com/article/10.1007/s10689-017-0030-x/fulltext.html

Reference46 articles.

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3. Haraldsdottir S, Hampel H, Wei L, Wu C, Frankel W, Bekaii-Saab T, de la Chapelle A, Goldberg RM (2014) Prostate cancer incidence in males with Lynch syndrome. Genet Med 16:553–5577. doi: 10.1038/gim.2013.193

4. Peltomäki P (2005) Lynch syndrome genes. Fam Cancer 4:227–232. doi: 10.1007/s10689-004-7993-0

5. Vasen HF, Blanco I, Aktan-Collan K, Gopie JP, Alonso A, Aretz S, Bernstein I, Bertario L, Burn J, Capella G, Colas C, Engel C, Frayling IM, Genuardi M, Heinimann K, Hes FJ, Hodgson SV, Karagiannis JA, Lalloo F, Lindblom A, Mecklin JP, Møller P, Myrhoj T, Nagengast FM, Parc Y, Ponz de Leon M, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Sijmons RH, Tejpar S, Thomas HJ, Rahner N, Wijnen JT, Järvinen HJ, Möslein G, Mallorca Group (2013) Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts. Gut 62:812–823. doi: 10.1136/gutjnl-2012-304356

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