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  1. Article

    Open Access

    Dorsal visual stream and LIMK1: hemideletion, haplotype, and enduring effects in children with Williams syndrome

    Williams syndrome (WS), a rare neurodevelopmental disorder caused by hemizygous deletion ofโ€‰~โ€‰25 genes from chromosomal band 7q11.23, affords an exceptional opportunity to study associations between a well-del...

    J. Shane Kippenhan, Michael D. Gregory in Journal of Neurodevelopmental Disorders (2023)