Haploinsufficiency of BAZ1B contributes to Williams syndrome through transcriptional dysregulation of neurodevelopmental pathways

Overview of attention for article published in Human Molecular Genetics, January 2016

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So far, Dimensions has found 60 publications that cite this research output.

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The most recent citing publications are shown below. View all 60 publications that cite this research output on Dimensions.

Molecular landscape of congenital vertebral malformations: recent discoveries and future directions

Article in Orphanet Journal of Rare Diseases (January 2024)

Disrupting fzd9b in zebrafish recapitulates stress- and anxiety-like behaviours associated with Williams syndrome

Preprint in bioRxiv (January 2024)

Epigenetic regulation of craniofacial development and disease

Article in Birth Defects Research (November 2023)

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