Paternally inherited WT1 mutation plus uniparental disomy of 11p may be an essential mechanism for development of WT1 ‐mutated familial Wilms tumor

Pediatric Blood&Cancer, EarlyView.

Source: Pediatric Blood and Cancer - September 17, 2018 Category: Cancer & Oncology Authors: YuyaSato , MasayukiHaruta , YasuhikoKaneko , YoshimasaNakasato , HidemitsuKurosawa , ShigemiYoshihara Source Type: research