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
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Citation Impact
MSK Authors
  1. Martin Stuart Tallman
    494 Tallman
  2. Ross Levine
    540 Levine
  3. Maria Eugenia Arcila
    459 Arcila
  4. Ahmet Dogan
    231 Dogan
  5. Mikhail Roshal
    92 Roshal
  6. Jacob Lowell Glass
    21 Glass
  7. Yanming Zhang
    59 Zhang
  8. Wenbin Xiao
    31 Xiao
  9. Jee Yeon Baik
    17 Baik
  10. Allison Marie Sigler
    9 Sigler
  11. Pallavi Kanwar Galera
    3 Galera