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

SIMPLE SUMMARY: Chromosomal abnormalities and somatic mutations are found in patients with myelodysplastic syndromes (MDS) and myelodysplastic/myeloproliferative neoplasms (MDS/MPN) in around 50–80% of cases. The identification of these alterations is important for the accurate diagnosis and prognos...

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Detalles Bibliográficos
Autores principales: Liquori, Alessandro, Lesende, Iván, Palomo, Laura, Avetisyan, Gayane, Ibáñez, Mariam, González-Romero, Elisa, Boluda-Navarro, Mireia, Morote-Faubel, Mireya, Garcia-Ruiz, Cristian, Martinez-Valiente, Cristina, Santiago-Balsera, Marta, Gomez-Seguí, Inés, Sanjuan-Pla, Alejandra, Sanz, Miguel A., Sanz, Guillermo, Solé, Francesc, Such, Esperanza, Cervera, José
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8072643/
https://www.ncbi.nlm.nih.gov/pubmed/33919541
http://dx.doi.org/10.3390/cancers13081947

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8072643/
https://www.ncbi.nlm.nih.gov/pubmed/33919541
http://dx.doi.org/10.3390/cancers13081947

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