Use of multilocus methylation-specific single nucleotide primer extension (MS-SNuPE) technology in diagnostic testing for human imprinted loci
Author:
Publisher
Informa UK Limited
Subject
Cancer Research,Molecular Biology
Link
http://www.tandfonline.com/doi/pdf/10.4161/epi.19719
Reference21 articles.
1. ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome;Arima;Nucleic Acids Res,2005
2. A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitus;Mackay;Hum Genet,2006
3. The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region;Rossignol;J Med Genet,2006
4. 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
5. Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells;Bliek;Eur J Hum Genet,2009
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