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WAGR Syndrome

2 Diseases & Disorders / 2 Eye Diseases, Hereditary / 2 Aniridia / WAGR Syndrome

2 Diseases & Disorders / 2 Eye Abnormalities / 2 Aniridia / WAGR Syndrome

2 Diseases & Disorders / 2 Uveal Diseases / 2 Iris Diseases / 2 Aniridia / WAGR Syndrome

 
  MeSH description: A contiguous gene syndrome associated with hemizygous deletions of chromosome region 11p13. The condition is marked by the combination of Wilms' tumor (W), Aniridia (A), Genitourinary abnormalities (G), and Mental retardation (R).
 
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  Atlas of Genetics and Cytogenetics in Oncology and Haematology /France/: WAGR (Wilms' Tumor/Aniridia/Genitourinary Anomalies/Mental Retardation Syndrome)

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