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Article

A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locus.

1 Mar 1997

Abstract excerpt

Nineteen patients were analysed by fluorescence in situ hybridisation (FISH) with selected 11p13 markers. They were examined because they had either isolated sporadic or familial aniridia, or aniridia with one or more of the WAGR (Wilms' tumour, aniridia, genital anomalies, and mental retardation) syndrome anomalies. The FISH markers from distal 11p13 were cosmids FO2121, PAX6 (aniridia), D11S324, and WT1 (Wilms'...

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Identifiers

PMID: 9132491
DOI: 10.1136/jmg.34.3.207

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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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A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locus.PMID 9132491Read ↗

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WAGR Syndrome: A Clinical Review of 54 CasesSemantic proximity Read ↗

The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus.Semantic proximity Read ↗

Population-based risk estimates of Wilms tumor in sporadic aniridia. A comprehensive mutation screening procedure of PAX6 identifies 80% of mutations in aniridia.Semantic proximity Read ↗

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