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Paper Details

ANKRD11 pathogenic variants and 16q24.3 microdeletions share an altered DNA methylation signature in patients with KBG syndrome.
Hum Mol Genet
6
2023
16q24, ANKRD11, ANKRD11 gene, ANKRD11 variants, Infinium EPIC array, KBG syndrome, KBGS, Syndromic conditions, ankyrin repeat-containing protein 11A, child, chromatin, differentially methylated CpG sites, epigenetic regulatory genes, inherited missense variant, intellectual disability, neurodevelopmental syndrome, patients, peripheral blood, skeletal anomalies, whole
Author NameAffiliation
Fowzan S AlkurayaCenter for Genomic Medicine, King Faisal Specialist Hospital and Research Center
Stephen W SchererResearch Institute, The Hospital for Sick Children
Stephen W SchererUniversity of Toronto
Stephen W SchererInstitute of Medical Sciences, University of Toronto
Stephen W SchererResearch Institute, The Hospital for Sick Children
Stephen W SchererUniversity of Toronto
Stephen W SchererInstitute of Medical Sciences, University of Toronto
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