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Genomic studies of multiple myeloma reveal an association between X chromosome alterations and genomic profile complexity.
Genes Chromosomes Cancer. 2017 Jan;56(1):18-27. doi: 10.1002/gcc.22397. Epub 2016 Aug 18.
Genes Chromosomes Cancer. 2017.
PMID: 27454822
Free article.
Exome copy number variation detection: Use of a pool of unrelated healthy tissue as reference sample.
Wenric S, Sticca T, Caberg JH, Josse C, Fasquelle C, Herens C, Jamar M, Max S, Gothot A, Caers J, Bours V.
Wenric S, et al. Among authors: sticca t.
Genet Epidemiol. 2017 Jan;41(1):35-40. doi: 10.1002/gepi.22019. Epub 2016 Nov 10.
Genet Epidemiol. 2017.
PMID: 27862228
Free article.
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Feasibility and clinical impact of routine molecular testing of gastrointestinal cancers at a tertiary centre with a multi-gene, tumor-agnostic, next generation sequencing panel.
Bregni G, Sticca T, Camera S, Akin Telli T, Craciun L, Trevisi E, Pretta A, Kehagias P, Leduc S, Senti C, Deleporte A, Vandeputte C, Saad ED, Kerger J, Gil T, Piccart-Gebhart M, Awada A, Demetter P, Larsimont D, Hendlisz A, Aftimos P, Sclafani F.
Bregni G, et al. Among authors: sticca t.
Acta Oncol. 2020 Dec;59(12):1438-1446. doi: 10.1080/0284186X.2020.1809704. Epub 2020 Aug 21.
Acta Oncol. 2020.
PMID: 32820683
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