Search Results - "ENTREKIN, R. E"

Extensive genomic abnormalities in childhood medulloblastoma by comparative genomic hybridization by REARDON, D. A, MICHALKIEWICZ, E, KUN, L. E, SHAPIRO, D. N, LOOK, A. T, BOYETT, J. M, SUBLETT, J. E, ENTREKIN, R. E, RAGSDALE, S. T, VALENTINE, M. B, BEHM, F. G, LI, H, HEIDEMAN, R. L

“…We analyzed 27 samples of primary medulloblastoma, using comparative genomic hybridization and a novel statistical approach to evaluate chromosomal regions for…”
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Chromosome arm 6q loss is the most common recurrent autosomal alteration detected in primary pediatric ependymoma by Reardon, David A., Entrekin, Ruth E., Sublett, Jack, Ragsdale, Susan, Li, Hao, Boyett, James, Kepner, James L., Look, A. Thomas

“…We analyzed 23 samples of primary pediatric ependymoma for significant gains or losses of genomic DNA, using comparative genomic hybridization (CGH) and a…”
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Chromosomal localization of the human smoothened gene (SMOH) to 7q32.3 by fluorescence in situ hybridization and radiation hybrid mapping by SUBLETT, J. E, ENTREKIN, R. E, LOOK, A. T, REARDON, D. A

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Chromosomal localization of the human smoothened gene (SMOH) to 7q32. 3 by fluorescence in situ hybridization and radiation hybrid mapping by Sublett, J E, Entrekin, R E, Look, A T, Reardon, D A

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