Microarray detection of multiple recurring submicroscopic chromosomal aberrations in pediatric T-cell acute lymphoblastic leukemia

L. Yu; M. L. Slovak; K. Mannoor; C. Chen; S. P. Hunger; A. J. Carroll; R. A. Schultz; L. G. Shaffer; B. C. Ballif; Y. Ning

doi:10.1038/leu.2011.33

Microarray detection of multiple recurring submicroscopic chromosomal aberrations in pediatric T-cell acute lymphoblastic leukemia

L. Yu^*, M. L. Slovak, K. Mannoor, C. Chen, S. P. Hunger, A. J. Carroll, R. A. Schultz, L. G. Shaffer, B. C. Ballif, Y. Ning

^*Corresponding author for this work

Pathology

Research output: Contribution to journal › Article › peer-review

15 Scopus citations

Original language	English (US)
Pages (from-to)	1042-1046
Number of pages	5
Journal	Leukemia
Volume	25
Issue number	6
DOIs	https://doi.org/10.1038/leu.2011.33
State	Published - Jun 2011

ASJC Scopus subject areas

Hematology
Oncology
Cancer Research

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10.1038/leu.2011.33

Cite this

@article{2c473987e16e447e9f621ef034edd51d,

title = "Microarray detection of multiple recurring submicroscopic chromosomal aberrations in pediatric T-cell acute lymphoblastic leukemia",

author = "L. Yu and Slovak, {M. L.} and K. Mannoor and C. Chen and Hunger, {S. P.} and Carroll, {A. J.} and Schultz, {R. A.} and Shaffer, {L. G.} and Ballif, {B. C.} and Y. Ning",

note = "Funding Information: We thank Children{\textquoteright}s Oncology Group Cell Bank for providing patient samples and thank the staff at Signature Genomic Laboratories (Victoria Cawich, Caitlin Valentin, Sara Minier, Nicholas Neill, and Steve Byerly) for their technical and graphic assistance. SPH is the Ergen Family Chair in Pediatric Cancer. This work was supported by grants CA30969, CA29139, CA98543, CA98413, and CA114766 awarded to the Children{\textquoteright}s Oncology Group.",

year = "2011",

month = jun,

doi = "10.1038/leu.2011.33",

language = "English (US)",

volume = "25",

pages = "1042--1046",

journal = "Leukemia",

issn = "0887-6924",

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}

Microarray detection of multiple recurring submicroscopic chromosomal aberrations in pediatric T-cell acute lymphoblastic leukemia. / Yu, L.; Slovak, M. L.; Mannoor, K.; Chen, C.; Hunger, S. P.; Carroll, A. J.; Schultz, R. A.; Shaffer, L. G.; Ballif, B. C.; Ning, Y.

In: Leukemia, Vol. 25, No. 6, 06.2011, p. 1042-1046.

Research output: Contribution to journal › Article › peer-review

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T1 - Microarray detection of multiple recurring submicroscopic chromosomal aberrations in pediatric T-cell acute lymphoblastic leukemia

AU - Yu, L.

AU - Slovak, M. L.

AU - Mannoor, K.

AU - Chen, C.

AU - Hunger, S. P.

AU - Carroll, A. J.

AU - Schultz, R. A.

AU - Shaffer, L. G.

AU - Ballif, B. C.

AU - Ning, Y.

N1 - Funding Information: We thank Children’s Oncology Group Cell Bank for providing patient samples and thank the staff at Signature Genomic Laboratories (Victoria Cawich, Caitlin Valentin, Sara Minier, Nicholas Neill, and Steve Byerly) for their technical and graphic assistance. SPH is the Ergen Family Chair in Pediatric Cancer. This work was supported by grants CA30969, CA29139, CA98543, CA98413, and CA114766 awarded to the Children’s Oncology Group.

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