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 (Q84563027)
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scientific article published on 14 September 2009
Language | Label | Description | Also known as |
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English | 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 |
scientific article published on 14 September 2009 |
Statements
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 (English)
Sylvie Rossignol
Virginie Steunou
Theo Sas
Nathalie Thibaud
Fabienne Danton
Maryline Le Jule
Claudine Heinrichs
Sylvie Cabrol
Christine Gicquel
Yves Le Bouc
Irene Netchine
14 September 2009