Next-generation sequencing improves precision medicine in hearing loss

por Imizcoz, T., Prieto-Matos, C., Manrique-Huarte, R., Calavia, D., Huarte, A., Pruneda, P. C., Ordoñez, G. R., Cañada-Higueras, E., Patiño-García, A., Alkorta-Aranburu, G., Manrique Rodríguez, M.
Publicado 2023

Clinical utility of gene panel-based testing for hereditary myelodysplastic syndrome/acute leukemia predisposition syndromes

por Guidugli, L, Johnson, A K, Alkorta-Aranburu, G, Nelakuditi, V, Arndt, K, Churpek, J E, Godley, L A, Townsley, D, Young, N S, Fitzpatrick, C, del Gaudio, D, Das, S, Li, Z
Publicado 2017