## INAUGURAL DR. ClULlO 1. D'ANGIO AWARD of adults who have been both cured of their tumor and In 1940, the diagnosis of Wilms' tumor was associated with the same poor prognosis as that of other forms of childhood cancer. The addition of radiation therapy, and then chemotherapy to the management
Mutations of APC gene and genes involved in beckwith-wiedemann syndrome are frequently found in children with hepatoblastoma
β Scribed by Montalto, G.; Cetta, F.; Negrini, M.; Schwienbacher, C.; Gori, M.; Acquaviva, A.; Morgese, G.
- Book ID
- 123309826
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- English
- Weight
- 319 KB
- Volume
- 114
- Category
- Article
- ISSN
- 0016-5085
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The Beckwith-Wiedemann syndrome (BWS) is an overgrowth malformation syndrome that occurs with an incidence of 1:13,700 births. There is a striking incidence of childhood tumors found in BWS patients. Various lines of investigation have localized "imprinted" genes involved in BWS and associated child
## Abstract The Turcot syndrome (TS) is a rare, probably autosomal recessive, disorder characterized by development of primary neuroepithelial tumors of the central nervous system (CNS) and numerous adenomatous colorectal polyps. To examine the possible involvement of mutations of the __APC__ gene,