Associated Papers
Custom multi‑tumor next‑generation sequencing panel for routine molecular diagnosis of solid tumors: Validation and results from three‑year clinical use.
Chevrier S et al.
International Journal of Molecular Medicine, 2022
35244186 (PubMed )
Supplement: Supplementary_Data2.xlsx › Feuil1
A comprehensive overview of FCGR3A gene variability by full-length gene sequencing including the identification of V158F polymorphism.
Mahaweni NM et al.
Scientific Reports, 2018
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