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Temporal and Clonal Progression in a Pediatric Ependymoma Patient Through Multiple Treatments
View ORCID ProfileChristopher A. Miller, Sonika Dahiya, Tiandao Li, Robert S. Fulton, Matthew D. Smyth, Gavin P. Dunn, Joshua B. Rubin, Elaine R. Mardis
doi: https://doi.org/10.1101/115923
Christopher A. Miller
1Department of Medicine, Division of Oncology, Washington University School of Medicine, St Louis, MO, United States
2McDonnell Genome Institute, Washington University School of Medicine, St Louis, Missouri, United States
Sonika Dahiya
3Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, United States
Tiandao Li
2McDonnell Genome Institute, Washington University School of Medicine, St Louis, Missouri, United States
Robert S. Fulton
2McDonnell Genome Institute, Washington University School of Medicine, St Louis, Missouri, United States
Matthew D. Smyth
4Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri
Gavin P. Dunn
4Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri
5Center for Human Immunology and Immunotherapy Programs, Washington University School of Medicine, St. Louis, Missouri, United States
Joshua B. Rubin
6Department of Pediatrics, Washington University School of Medicine, St Louis, Missouri, United States
Elaine R. Mardis
7Institute for Genomic Medicine, Nationwide Children’s Hospital, and The Ohio State University College of Medicine, Columbus, Ohio, United States
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Posted March 11, 2017.
Temporal and Clonal Progression in a Pediatric Ependymoma Patient Through Multiple Treatments
Christopher A. Miller, Sonika Dahiya, Tiandao Li, Robert S. Fulton, Matthew D. Smyth, Gavin P. Dunn, Joshua B. Rubin, Elaine R. Mardis
bioRxiv 115923; doi: https://doi.org/10.1101/115923
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