MeSH tree: C10.597.613.575
Global partnerships that embed scientific research into clinical care are revolutionizing the diagnosis and treatments for children with rare genetic diseases, according to a new report.
Feb 27, 2025
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A clinical research team from the LKS Faculty of Medicine, the University of Hong Kong (HKUMed), and international genetic researchers led a global research study using multi-omics analysis and identified a novel gene, DDX39B, ...
Feb 21, 2025
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In a new study, UCLA Health researchers have found that motor delay and low muscle tone were common signs of an underlying genetic diagnosis in children with neurodevelopment disorders.
Oct 11, 2024
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