MeSH tree: C14.280.484.048.750.535
Researchers who lead the world's first comprehensive sequencing program for newborn infants have published the next chapter in the ongoing study of the BabySeq Project, with new findings on infants and families who have been ...
Jun 5, 2023
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A new study by the Tel Aviv and Hebrew Universities found that abnormal processes lead to disruption in the expression of genes essential for brain development in people suffering from Williams syndrome—a rare, multisystem ...
Jan 16, 2023
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Using an in vivo model that mimics the genetic alteration of Williams-Beuren syndrome, researchers from the UPF's Neuropharmacology Laboratory—NeuroPhar, in collaboration with several other universities, found alterations ...
Oct 12, 2022
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Williams-Beuren syndrome (WBS) is a rare disorder that causes neurocognitive and developmental deficits. However, musical and auditory abilities are preserved or even enhanced in WBS patients. Scientists at St. Jude Children's ...
Sep 23, 2022
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