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

✍ Scribed by Le Jule, M.; Heinrichs, C.; Cabrol, S.; Gicquel, C.; Azzi, S.; Rossignol, S.; Steunou, V.; Sas, T.; Thibaud, N.; Danton, F.

• Book ID: 115475937
• Publisher: Oxford University Press
• Year: 2009
• Tongue: English
• Weight: 230 KB
• Volume: 18
• Category: Article
• ISSN: 0964-6906
• DOI: 10.1093/hmg/ddp435