Potential benefits of rapid genetic testing for germline WT1 in infants with bilateral renal tumors: A case report
Author:
Affiliation:
1. Department of Pediatrics Keio University School of Medicine Tokyo Japan
2. The Center for Differences of Sex Development Keio University Hospital Tokyo Japan
3. Department of Urology Keio University School of Medicine Tokyo Japan
Publisher
Wiley
Subject
Oncology,Hematology,Pediatrics, Perinatology and Child Health
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.29368
Reference12 articles.
1. Results of the First Prospective Multi-institutional Treatment Study in Children With Bilateral Wilms Tumor (AREN0534)
2. Current Issues in Wilms Tumor Management
3. A Case of Bilateral Cystic Partially Differentiated Nephroblastoma vs Cystic Wilms' Tumor: Highlighting a Diagnostic Dilemma
4. A high incidence of WT1 abnormality in bilateral Wilms tumours in Japan, and the penetrance rates in children with WT1 germline mutation
5. Wilms tumour surveillance in at-risk children: Literature review and recommendations from the SIOP-Europe Host Genome Working Group and SIOP Renal Tumour Study Group
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