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

doi:10.1016/j.cancergencyto.2009.03.004

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 journal › Letter › peer-review

2 Scopus citations

Original language	English (US)
Pages (from-to)	67-69
Number of pages	3
Journal	Cancer Genetics and Cytogenetics
Volume	193
Issue number	1
DOIs	https://doi.org/10.1016/j.cancergencyto.2009.03.004
State	Published - Aug 1 2009

ASJC Scopus subject areas

Molecular Biology
Genetics
Cancer Research

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10.1016/j.cancergencyto.2009.03.004

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@article{d2117093fde84aab9e3d7fa6855a6a20,

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

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

year = "2009",

month = aug,

day = "1",

doi = "10.1016/j.cancergencyto.2009.03.004",

language = "English (US)",

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T1 - Acute myeloid leukemia (M2) with a cryptic RUNX1/RUNX1T1 t(1;21;8)(p36;q22;q22) variant

AU - Tirado, Carlos A.

AU - Chen, Weina

AU - Valdez, Federico J.

AU - Henderson, Samuel

AU - Doolittle, Jeff

AU - Garcia, Rolando

AU - Patel, Sangeeta

AU - Holdridge, Scott

AU - Chastain, Candace

AU - Collins, Robert H.

PY - 2009/8/1

Y1 - 2009/8/1

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U2 - 10.1016/j.cancergencyto.2009.03.004

DO - 10.1016/j.cancergencyto.2009.03.004

M3 - Letter

C2 - 19602466

AN - SCOPUS:67651089840

SN - 0165-4608

VL - 193

SP - 67

EP - 69

JO - Cancer Genetics and Cytogenetics

JF - Cancer Genetics and Cytogenetics

IS - 1

ER -

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

ASJC Scopus subject areas

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