Tumor risk in Beckwith-Wiedemann syndrome: A review and meta-analysis
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference58 articles.
1. Children at increased risk for Wilms tumor: Monitoring issues
2. Single cell analysis demonstrating somatic mosaicism involving 11p in a patient with paternal isodisomy and Beckwith—Wiedemann syndrome
3. Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS
4. RENAL FINDINGS ON RADIOLOGICAL FOLLOWUP OF PATIENTS WITH BECKWITH-WIEDEMANN SYNDROME
5. Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway
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