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Unique Molecular Characteristics of Pediatric Myxopapillary Ependymoma
Article first published online: 10 SEP 2009
© 2009 The Authors; Journal Compilation © 2009 International Society of Neuropathology
Volume 20, Issue 3, pages 560–570, May 2010
How to Cite
Barton, V. N., Donson, A. M., Kleinschmidt-DeMasters, B. K., Birks, D. K., Handler, M. H. and Foreman, N. K. (2010), Unique Molecular Characteristics of Pediatric Myxopapillary Ependymoma. Brain Pathology, 20: 560–570. doi: 10.1111/j.1750-3639.2009.00333.x
- Issue published online: 12 APR 2010
- Article first published online: 10 SEP 2009
- Received 22 June 2009; accepted 26 August 2009.
Table S1. Cohort demographics including patient diagnosis, age at diagnosis, gender and tumor grade. Grade denotes the histological grade as defined by the World Health Organization classification of tumors of the central nervous system. The table indicates if specimens were included in the gene expression microarray or immunohistochemistry cohorts (Microarray or IHC, respectively). Abbreviations: dx = diagnosis; MEPN = myxopapillary ependymoma; ST EPN = supratentorial ependymoma; IF EPN = infratentorial ependymoma; SP EPN = spinal ependymoma; SEPN = subependymoma; NE = normal ependyma (spinal cord sections); M = male; F = female; Y = yes; N = no.
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