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

  1. Liquori, A.
  2. Lesende, I.
  3. Palomo, L.
  4. Avetisyan, G.
  5. Ibáñez, M.
  6. González-Romero, E.
  7. Boluda-Navarro, M.
  8. Morote-Faubel, M.
  9. Garcia-Ruiz, C.
  10. Martinez-Valiente, C.
  11. Santiago-Balsera, M.
  12. Gomez-Seguí, I.
  13. Sanjuan-Pla, A.
  14. Sanz, M.A.
  15. Sanz, G.
  16. Solé, F.
  17. Such, E.
  18. Cervera, J.
Journal:
Cancers

ISSN: 2072-6694

Year of publication: 2021

Volume: 13

Issue: 8

Type: Article

DOI: 10.3390/CANCERS13081947 GOOGLE SCHOLAR lock_openOpen access editor

Sustainable development goals

Data source: Scopus