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  • Search Condition : Filter (MeSH = Developmental Disabilities / genetics)
Species Resource Title
Human and Animal Cells 293T(RCB2202) A chromosome 16p13.11 microduplication causes hyperactivity through dysregulation of miR-484/protocadherin-19 signaling.
Zebrafish isl1:GFP/rw0 EXOSC8 mutations alter mRNA metabolism and cause hypomyelination with spinal muscular atrophy and cerebellar hypoplasia.