1. A Single Next-Generation Sequencing (NGS) Assay for the Detection of Point Mutations and Large Chromosomal Abnormalities in MDS Patients. (April 2017) Authors: Liquori, A.; Such, E.; Palomo, L.; Moreau, S.; Pedrola, L.; Sellés, J.; Neef, A.; Zúñiga, S.; Ibáñez, M.; Company, D.; Saus, A.; Acha, P.; Sanjuan-Pla, A.; Boluda, M.; de Matteo, B.; González, E.; Sanz, M.A.; Solé, F.; Sanz, G.; Cervera, J. Journal: Leukemia research Issue: Volume 55(2017)Supplement 1 Page Start: S18 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗