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Human Mutation|July 22, 2014
Complex tissue-specific epigenotypes in Russell-Silver Syndrome associated with 11p15 ICR1 hypomethylationSalah Azzi, Annick Blaise, Virginie Steunou, et al.Human Molecular Genetics|June 12, 2014
Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndromeWalid Abi Habib, Salah Azzi, Frédéric Brioude, et al.Nature Communications|July 7, 2025
High-coverage allele-resolved single-cell DNA methylation profiling reveals cell lineage, X-inactivation state, and replication dynamicsNathan J Spix, Walid Abi Habib, Zhouwei Zhang, 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