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Article

The role of Wilms' tumor genes.

The journal of medical investigation : JMI - 1 Aug 1999

Hirose M

Abstract excerpt

The constitutional chromosomal deletion within the short arm of one copy of chromosome 11, at band p13, which often correlated with WAGR syndrome consisting of Wilms' tumor with aniridia, genitourinary malformation, and mental retardation, provided the first clue to the genetic events in the development of Wilms' tumor. WT1 gene is encoded by 10 exons, resulting in messenger RNA subject to a complex pattern of...

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PMID: 10687307

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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WT1: a novel tumor suppressor gene inactivated in Wilms' tumor.Semantic proximity Read ↗

Wilms' tumor gene 1 in hematological malignancies: friend or foe?Semantic proximity Read ↗

The genetic factors contributing to the development of Wilm's tumor and their clinical utility in its diagnosis and prognosis.Semantic proximity Read ↗

The WT1 Wilms tumor gene product: a developmentally regulated transcription factor in the kidney that functions as a tumor suppressorSemantic proximity Read ↗

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