Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith–Wiedemann syndrome
✍ Scribed by Gaston, Véronique; Le Bouc, Yves; Soupre, Véronique; Burglen, Lydie; Donadieu, Jeam; Oro, Hubert; Audry, Georges; Vazquez, Marie-Paule; Gicquel, Christine
- Book ID
- 110025133
- Publisher
- Nature Publishing Group
- Year
- 2001
- Tongue
- English
- Weight
- 279 KB
- Volume
- 9
- Category
- Article
- ISSN
- 1018-4813
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## 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
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