Frequent RUNX1 and TP53 mutations in secondary acute myeloid leukemia with mixed phenotype Meeting Abstract
| Authors: | Galera, P.; Baik, J.; Famulare, C.; Sigler, A.; Zhang, Y.; Arcila, M.; Dogan, A.; Tallman, M.; Levine, R.; Glass, J.; Roshal, M.; Xiao, W. |
| Abstract Title: | Frequent RUNX1 and TP53 mutations in secondary acute myeloid leukemia with mixed phenotype |
| Meeting Title: | 109th Annual Meeting of the United States and Canadian Academy of Pathology (USCAP) |
| Journal Title: | Laboratory Investigation |
| Volume: | 100 |
| Issue: | Suppl. 1 |
| Meeting Dates: | 2020 Feb 29-Mar 5 |
| Meeting Location: | Los Angeles, CA |
| ISSN: | 0023-6837 |
| Publisher: | Nature Publishing Group |
| Date Published: | 2020-03-01 |
| Start Page: | 1293 |
| End Page: | 1294 |
| Language: | English |
| ACCESSION: | WOS:000518328803057 |
| PROVIDER: | wos |
| PUBMED: | 32139860 |
| DOI: | 10.1038/s41374-020-0391-x |
| Notes: | Meeting Abstract: 1372 -- Source: Wos |
