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.
Revista:
Cancers

ISSN: 2072-6694

Ano de publicación: 2021

Volume: 13

Número: 8

Tipo: Artigo

DOI: 10.3390/CANCERS13081947 GOOGLE SCHOLAR lock_openAcceso aberto editor