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 journalArticle

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

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Core Binding Factor Alpha 2 Subunit
Chromosomes, Human, Pair 21
Chromosomes, Human, Pair 8
Genetic Translocation
Chromosomes, Human, Pair 1
Acute Myeloid Leukemia

ASJC Scopus subject areas

  • Cancer Research
  • Genetics
  • Molecular Biology

Cite this

Acute myeloid leukemia (M2) with a cryptic RUNX1/RUNX1T1 t(1;21;8)(p36;q22;q22) variant. / Tirado, Carlos A.; Chen, Weina; Valdez, Federico J.; Henderson, Samuel; Doolittle, Jeff; Garcia, Rolando; Patel, Sangeeta; Holdridge, Scott; Chastain, Candace; Collins, Robert H.

In: Cancer Genetics and Cytogenetics, Vol. 193, No. 1, 08.2009, p. 67-69.

Research output: Contribution to journalArticle

Tirado, CA, Chen, W, Valdez, FJ, Henderson, S, Doolittle, J, Garcia, R, Patel, S, Holdridge, S, Chastain, C & Collins, RH 2009, 'Acute myeloid leukemia (M2) with a cryptic RUNX1/RUNX1T1 t(1;21;8)(p36;q22;q22) variant', Cancer Genetics and Cytogenetics, vol. 193, no. 1, pp. 67-69. https://doi.org/10.1016/j.cancergencyto.2009.03.004
Tirado, Carlos A. ; Chen, Weina ; Valdez, Federico J. ; Henderson, Samuel ; Doolittle, Jeff ; Garcia, Rolando ; Patel, Sangeeta ; Holdridge, Scott ; Chastain, Candace ; Collins, Robert H. / Acute myeloid leukemia (M2) with a cryptic RUNX1/RUNX1T1 t(1;21;8)(p36;q22;q22) variant. In: Cancer Genetics and Cytogenetics. 2009 ; Vol. 193, No. 1. pp. 67-69.
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