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Panel Sequencing for Clinically Oriented Variant Screening and Copy Number Detection in Chronic Lymphocytic Leukemia Patients.
Diagnostics (Basel). 2022 Apr 11;12(4):953. doi: 10.3390/diagnostics12040953.
Diagnostics (Basel). 2022.
PMID: 35454001
Free PMC article.
A Single-Run Next-Generation Sequencing (NGS) Assay for the Simultaneous Detection of Both Gene Mutations and Large Chromosomal Abnormalities in Patients with Myelodysplastic Syndromes (MDS) and Related Myeloid Neoplasms.
Liquori A, Lesende I, Palomo L, Avetisyan G, Ibáñez M, González-Romero E, Boluda-Navarro M, Morote-Faubel M, Garcia-Ruiz C, Martinez-Valiente C, Santiago-Balsera M, Gomez-Seguí I, Sanjuan-Pla A, Sanz MA, Sanz G, Solé F, Such E, Cervera J.
Liquori A, et al. Among authors: morote faubel m.
Cancers (Basel). 2021 Apr 18;13(8):1947. doi: 10.3390/cancers13081947.
Cancers (Basel). 2021.
PMID: 33919541
Free PMC article.
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