A new strategy to screen MMR genes in Lynch Syndrome: HA-CAE, MLPA and RT-PCR
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Oncology
Reference37 articles.
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2. The incidence of Lynch syndrome;De la Chapelle;Fam Cancer,2005
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4. MSH2 genomic deletions are a frequent cause of HNPCC;Wijnen;Nat Genet,1998
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1. Diagnostics of Mutations in MMR/EPCAM Genes and Their Role in the Treatment and Care of Patients with Lynch Syndrome;Diagnostics;2020-10-05
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3. ReCAP: Oncologists’ Selection of Genetic and Molecular Testing in the Evolving Landscape of Stage II Colorectal Cancer;Journal of Oncology Practice;2016-03
4. Functional examination of MLH1, MSH2, and MSH6 intronic mutations identified in Danish colorectal cancer patients;BMC Medical Genetics;2013-10-03
5. Frequency and Variability of Genomic Rearrangements on MSH2 in Spanish Lynch Syndrome Families;PLoS ONE;2013-09-11
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