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  • Molecular assay reagents intended to identify deletions or duplications of the twist family bHLH transcription factor 1 (TWIST1) gene, located at chromosome 7p21.1, which encodes the protein twist-related protein 1. Genetic variants at this locus have been associated with craniosynostosis, Robinow Sorauf syndrome, and Saethre-Chotzen syndrome.
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