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
Salah Azzi(Inserm), Irène Netchine(Inserm), Theo Sas(Erasmus MC - Sophia Children’s Hospital), Sylvie Rossignol(Université de Limoges), Yves Le Bouc(Inserm), Virginie Steunou(Inserm), Fabienne Danton(Inserm), Nathalie Thibaud(Inserm), Christine Gicquel(Inserm), Maryline Le Jule(Inserm), Sylvie Cabrol(Hôpital d'Enfants), Claudine Heinrichs(Queen Fabiola Children's University Hospital)
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