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The Journal of Clinical Endocrinology and Metabolism|May 17, 2007
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 correlationsIrène Netchine, Sylvie Rossignol, Marie-Noëlle Dufourg, et al.Human Reproduction (Oxford, England)|December 14, 2020
Insights from the genetic characterization of central precocious puberty associated with multiple anomaliesAna Pinheiro Machado Canton, Ana Cristina Victorino Krepischi, Luciana Ribeiro Montenegro, et al.Science Advances|December 17, 2025
RIPK1 inhibition reduces biliary injury and fibrosis in primary sclerosing cholangitisPierre-Antoine Soret, Virginie Steunou, Julien Hedou, et al.Journal of Medical Genetics|October 7, 2019
Increasing knowledge in <i>IGF1R</i> defects: lessons from 35 new patientsEloïse Giabicani, Marjolaine Willems, Virginie Steunou, et al.The Journal of Clinical Endocrinology and Metabolism|April 17, 2018
Chromosome 14q32.2 Imprinted Region Disruption as an Alternative Molecular Diagnosis of Silver-Russell SyndromeSophie Geoffron, Walid Abi Habib, Sandra Chantot-Bastaraud, et al.Pageof 2