New-generation sequencing is already in routine clinical use, notably for the search of actionable mutations in oncology, and for non-invasive prenatal diagnostics. More applications are developing and will soon enter clinical practice. © 2014 médecine/sciences - Inserm.
CITATION STYLE
Jordan, B. (2014). Les retombées cliniques du séquençage de nouvelle génération: Chroniques gánomiques. Medecine/Sciences, 30(5), 589–593. https://doi.org/10.1051/medsci/20143005025
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