Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype

Migliorini, G, Fiege, B, Hosking, FJ, Ma, Y, Kumar, R, Sherborne, AL, da Silva Filho, MI, Vijayakrishnan, J, Koehler, R, Thomsen, H et al, Irving, JA, Allan, JM, Lightfoot, T, Roman, E, Kinsey, SE, Sheridan, E, Thompson, P, Hoffmann, P, Noethen, MM, Muehleisen, TW, Eisele, L, Zimmermann, M, Bartram, CR, Schrappe, M, Greaves, M, Stanulla, M, Hemminki, K and Houlston, RS (2013) Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype BLOOD, 122 (19). pp. 3298-3307.

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Item Type:	Article
Authors :	Name Email ORCID Migliorini, G Fiege, B Hosking, FJ Ma, Y y.ma@surrey.ac.uk Kumar, R Sherborne, AL da Silva Filho, MI Vijayakrishnan, J Koehler, R Thomsen, H Irving, JA Allan, JM Lightfoot, T Roman, E Kinsey, SE Sheridan, E Thompson, P Hoffmann, P Noethen, MM Muehleisen, TW Eisele, L Zimmermann, M Bartram, CR Schrappe, M Greaves, M Stanulla, M Hemminki, K Houlston, RS
Date :	7 November 2013
Identification Number :	10.1182/blood-2013-03-491316
Uncontrolled Keywords :	Science & Technology, Life Sciences & Biomedicine, Hematology, HEMATOLOGY, GENOME-WIDE ASSOCIATION, HUMAN BREAST-TUMORS, SUSCEPTIBILITY LOCI, POPULATION, VARIANTS, GATA3, SCHIZOPHRENIA, CHILDREN, SEQUENCE, PIP5K2A
Related URLs :	Author
Depositing User :	Symplectic Elements
Date Deposited :	17 May 2017 13:07
Last Modified :	17 May 2017 15:09
URI:	http://epubs.surrey.ac.uk/id/eprint/838021

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