“Epigenetic Signatures”
March 13, 2018 | Terry Sharrer
Kabuki syndrome is a rare inborn developmental disorder in children, with distinctive facial features, growth delays and other abnormalities. Yet it shares genetics with several other syndromes with strange names—CHARGE, Floating harbor, ATRX, Sotos, et al. Researchers at the Greenwood Genetic Center (Greenville, SC), however, have found that while these syndromes are genetically and clinically similar, methylation array analysis shows them to be quite distinguishable. MORE
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