Publications by authors named "Fabienne Danton"

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Implementation of a Reliable Next-Generation Sequencing Strategy for Molecular Diagnosis of Dystrophinopathies.
Melissa Alame, Delphine Lacourt, Reda Zenagui, Déborah Mechin, Fabienne Danton

J Mol Diagn· September 2016

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Allele-specific methylated multiplex real-time quantitative PCR (ASMM RTQ-PCR), a powerful method for diagnosing loss of imprinting of the 11p15 region in Russell Silver and Beckwith Wiedemann syndromes.
Salah Azzi, Virginie Steunou, Alexandra Rousseau, Sylvie Rossignol, Nathalie Thibaud, Fabienne Danton

Hum Mutat· February 2011

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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, Sylvie Rossignol, Virginie Steunou, Theo Sas, Nathalie Thibaud, Fabienne Danton

Hum Mol Genet· December 2009

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11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations.
Irène Netchine, Sylvie Rossignol, Marie-Noëlle Dufourg, Salah Azzi, Alexandra Rousseau, Fabienne Danton

J Clin Endocrinol Metab· August 2007

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Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome.
Christine Gicquel, Sylvie Rossignol, Sylvie Cabrol, Muriel Houang, Virginie Steunou, Fabienne Danton

Nat Genet· September 2005

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