Methylation analysis in tongue tissue of BWS patients identifies the (EPI)genetic cause in 3 patients with normal methylation levels in blood
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference17 articles.
1. Determination of KCNQ1OT1 and H19 methylation levels in BWS and SRS patients using methylation-sensitive high-resolution melting analysis;Alders;Eur J Hum Genet,2009
2. Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS;Bliek;Hum Mol Genet,2001
3. Risk of cancer during the first four years of life in children from The Beckwith-Wiedemann Syndrome Registry;DeBaun;J Pediatr,1998
4. Beckwith–Wiedemann syndrome: historical, clinicopathological, and etiopathogenetic perspectives;Cohen;Pediatr Dev Pathol,2005
5. Clinical features and natural history of Beckwith–Wiedemann syndrome: presentation of 74 new cases;Elliott;Clin. Genet.,1994
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