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

Author： Azzi Salah   Rossignol Sylvie   Steunou Virginie   Sas Theo   Thibaud Nathalie   Danton Fabienne   Le Jule Maryline   Heinrichs Claudine   Cabrol Sylvie   Gicquel Christine   Le Bouc Yves   Netchine Irene  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.18, Iss.24, 2009-12, pp. : 4724-4733

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