Primary leptomeningeal oligodendroglioma with documented progression to anaplasia and t(1;19)(q10;p10) in a child. [electronic resource]
Producer: 20091008Description: 575-7 p. digitalISSN:- 1432-0533
- Anaplasia -- genetics
- Child, Preschool
- Chromosome Deletion
- Chromosomes, Human, Pair 1 -- genetics
- Chromosomes, Human, Pair 19 -- genetics
- Disease Progression
- Female
- Humans
- Magnetic Resonance Imaging
- Meningeal Neoplasms -- genetics
- Oligodendroglioma -- genetics
- Spinal Cord -- pathology
- Translocation, Genetic
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Publication Type: Case Reports; Journal Article
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