1. Genomic analysis of a familial myelodysplasia/acute myeloid leukemia and inherited RUNX1 mutations without a pre-existing platelet disorder. Issue 1 (2nd January 2020) Authors: Prieto-Conde, María Isabel; Labrador, Jorge; Hermida, Gerardo; Alonso, Sara; Jiménez, Cristina; García-Álvarez, María; Medina, Alejandro; Balanzategui, Ana; Alcoceba, Miguel; Sarasquete, María Eugenia; Puig, Noemí; González, Verónica; Gutiérrez, Norma C.; García-Sanz, Ramón; González-Díaz, Marcos... Journal: Leukemia & lymphoma Issue: Volume 61:Issue 1(2020) Page Start: 181 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Reply to Brown et al: 'Correct application of variant classification guidelines in germline RUNX1 mutated disorders to assist clinical diagnosis'. Issue 1 (2nd January 2020) Authors: Prieto-Conde, María Isabel; Labrador, Jorge; Hermida, Gerardo; Alonso, Sara; Jiménez, Cristina; García-Alvarez, María; Medina, Alejandro; Balanzategui, Ana; Alcoceba, Miguel; Sarasquete, María Eugenia; Puig, Noemí; González, Verónica; Gutiérrez, Norma C.; García-Sanz, Ramón; González-Díaz, Marcos... Journal: Leukemia & lymphoma Issue: Volume 61:Issue 1(2020) Page Start: 248 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗