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Bilateral preaxial polydactyly in a WAGR syndrome patient

✍ Scribed by Siranoush Manoukian; John A. Crolla; Palma M.A. Mammoliti; Maria Adele Testi; Rinaldo Zanini; Maria Luisa Carpanelli; Elena Piozzi; Gabriella Sozzi; Giovanna De Vecchi; Monica Terenziani; Filippo Spreafico; Paola Collini; Paolo Radice; Daniela Perotti

Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
139 KB
Volume
134A
Category
Article
ISSN
1552-4825

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## Abstract Wilms tumor, aniridia, genitourinary anomalies, and mental retardation (WAGR) syndrome is a contiguous gene deletion syndrome involving the Wilms tumor 1 gene (__WT1__), the paired box gene 6 (__PAX6__), and possibly other genes on chromosome 11p13. __WT1__ is required for normal format