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Publications by Stefan Aretz

Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-Tumor Phenotype

Cancer Cell
Cancer ResearchOncologyCell Biology
2019English

Copy Number Variation Analysis and Targeted NGS in 77 Families With Suspected Lynch Syndrome Reveals Novel Potential Causative Genes

International Journal of Cancer
Cancer ResearchOncology
2018English

Diagnostic Yield and Clinical Utility of a Comprehensive Gene Panel for Hereditary Tumor Syndromes

Hereditary Cancer in Clinical Practice
OncologyGenetics
2019English

Chromoendoscopy in Combination With Random Biopsies Does Not Improve Detection of Gastric Cancer Foci in CDH1 Mutation Positive Patients

Endoscopy International Open
2016English

BRAF Mutation Testing of MSI CRCs in Lynch Syndrome Diagnostics: Performance and Efficiency According to Patient`s Age

2019English

Planning the Human Variome Project: The Spain Report

Human Mutation
Genetics
2009English

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