Paternally inherited WT1 mutation plus uniparental disomy of 11p may be an essential mechanism for development of WT1-mutated familial Wilms tumor.
Yuya SatoMasayuki HarutaYasuhiko KanekoYoshimasa NakasatoHidemitsu KurosawaShigemi YoshiharaPublished in: Pediatric blood & cancer (2018)
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