We have shown that an i(17q) is the most frequent abnormality in central nervous system primitive neuroectodermal tumors (PNETs; medulloblastoma), implicating the presence of a tumor suppressor gene which maps to 17p. In the present study, we investigated whether the deletion of chromosome arm 17p t
Low-grade Bone Lesions in Survivors of Childhood Medulloblastoma/Primitive Neuroectodermal Tumor
β Scribed by Koral, Korgun; Roy, Dave; Timmons, Charles F.; Gargan, Lynn; Bowers, Daniel C.
- Book ID
- 121809036
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- English
- Weight
- 776 KB
- Volume
- 19
- Category
- Article
- ISSN
- 1076-6332
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