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Comprehensive Constitutional Genetic and Epigenetic Characterization of Lynch-Like Individuals.
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- Cancers, 2020, v. 12, n. 7, p. 1799, doi. 10.3390/cancers12071799
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- Article
Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients.
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- Cancers, 2020, v. 12, n. 4, p. 829, doi. 10.3390/cancers12040829
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- Article
MLH1 methylation screening is effective in identifying epimutation carriers.
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- European Journal of Human Genetics, 2012, v. 20, n. 12, p. 1256, doi. 10.1038/ejhg.2012.136
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- Article
Genetic Screening for TLR7 Variants in Young and Previously Healthy Men With Severe COVID-19.
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- Frontiers in Immunology, 2021, v. 12, p. 1, doi. 10.3389/fimmu.2021.719115
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- Article
New insights into POLE and POLD1 germline mutations in familial colorectal cancer and polyposis.
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- Human Molecular Genetics, 2014, v. 23, n. 13, p. 3506, doi. 10.1093/hmg/ddu058
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- Article
Elucidating the molecular basis of MSH2-deficient tumors by combined germline and somatic analysis.
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- International Journal of Cancer, 2017, v. 141, n. 7, p. 1365, doi. 10.1002/ijc.30820
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- Article
Highly sensitive MLH1 methylation analysis in blood identifies a cancer patient with low-level mosaic MLH1 epimutation.
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- Clinical Epigenetics, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13148-019-0762-6
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- Article
Comprehensive analysis and ACMG‐based classification of CHEK2 variants in hereditary cancer patients.
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- Human Mutation, 2020, v. 41, n. 12, p. 2128, doi. 10.1002/humu.24110
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- Article
Identification of Two Novel EPOR Gene Variants in Primary Familial Polycythemia: Case Report and Literature Review.
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- Genes, 2022, v. 13, n. 10, p. N.PAG, doi. 10.3390/genes13101686
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- Article