𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Clinical Outcomes of Children and Adults With Central Nervous System Primitive Neuroectodermal Tumors

✍ Scribed by Lester, R.; Brown, L.; Foote, R.; Laack, N.


Book ID
122397072
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
55 KB
Volume
86
Category
Article
ISSN
0360-3016

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Mutation analysis and loss of heterozygo
✍ Irene Slavc; Ignacio R. Rodriguez; Krzysztof Mazuruk; Gerald J. Chader; Jaclyn A πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 French βš– 120 KB πŸ‘ 2 views

Deletion of 17p is the most frequent abnormality observed in central nervous system (CNS) primitive neuroectodermal tumors (PNETs), implicating the presence of a tumor suppressor gene which maps to 17p. The gene for pigment epitheliumderived factor (PEDF) has been cloned and mapped to 17p13. PEDF be