Molecular characterization reveals NF1 deletions and FGFR1 -activating mutations in a pediatric spinal oligodendroglioma-Reference-Cited by-同舟云学术

Molecular characterization reveals NF1 deletions and FGFR1 -activating mutations in a pediatric spinal oligodendroglioma

Author:

Bruzek Amy K.¹,Zureick Andrew H.²,McKeever Paul E.³,Garton Hugh J. L.¹,Robertson Patricia L.⁴,Mody Rajen⁵,Koschmann Carl J.⁵

Affiliation:

1. Department of Neurosurgery; University of Michigan Medical School; Ann Arbor Michigan

2. Medical School; University of Michigan Medical School; Ann Arbor Michigan

3. Department of Pathology; University of Michigan Medical School; Ann Arbor Michigan

4. Division of Pediatric Neurology; Department of Pediatrics; University of Michigan Medical School; Ann Arbor Michigan

5. Division of Pediatric Hematology/Oncology; Department of Pediatrics; University of Michigan Medical School; Ann Arbor Michigan

Funder

NIH/NICHD K12

University of Michigan Janette Ferrantino Investigator Award

National Institutes of Health Clinical Sequencing Exploratory Research Award

National Institute of Child Health and Human Development

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Reference21 articles.

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