[Disorders of sex development 46 XY and bilateral metachronous wilms tumor in a child with mutation in exon 7 of WT1 gene]. [electronic resource]

By: Contributor(s): Producer: 20200210Description: 109-112 p. digitalISSN:
  • 1728-2985
Subject(s): In: Urologiia (Moscow, Russia : 1999) no. 6
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Publication Type: Case Reports; Journal Article

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