Molecular Findings in Beckwith-Wiedemann Syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.c.31363/fullpdf
Reference112 articles.
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2. Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome;Arboleda;Nat Genet,2012
3. Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci;Azzi;Hum Mol Genet,2009
4. Allele-specific methylated multiplex real-time quantitative PCR (ASMM RTQ-PCR), a powerful method for diagnosing loss of imprinting of the 11p15 region in Russell Silver and Beckwith Wiedemann syndromes;Azzi;Hum Mutat,2011
5. A novel H19 antisense RNA overexpressed in breast cancer contributes to paternal IGF2 expression;Berteaux;Mol Cell Biol,2008
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