Acute myeloid leukemia (M2) with a cryptic RUNX1/RUNX1T1 t(1;21;8)(p36;q22;q22) variant

Carlos A. Tirado, Weina Chen, Federico J. Valdez, Samuel Henderson, Jeff Doolittle, Rolando Garcia, Sangeeta Patel, Scott Holdridge, Candace Chastain, Robert H. Collins

Research output: Contribution to journalLetter

2 Scopus citations
Original languageEnglish (US)
Pages (from-to)67-69
Number of pages3
JournalCancer Genetics and Cytogenetics
Volume193
Issue number1
DOIs
StatePublished - Aug 1 2009

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research

Cite this

Tirado, C. A., Chen, W., Valdez, F. J., Henderson, S., Doolittle, J., Garcia, R., Patel, S., Holdridge, S., Chastain, C., & Collins, R. H. (2009). Acute myeloid leukemia (M2) with a cryptic RUNX1/RUNX1T1 t(1;21;8)(p36;q22;q22) variant. Cancer Genetics and Cytogenetics, 193(1), 67-69. https://doi.org/10.1016/j.cancergencyto.2009.03.004