Cite

    Douglas, G., Cho, M. T., Telegrafi, A., Winter, S., Carmichael, J., Zackai, E. H., Deardorff, M. A., Harr, M., Williams, L., Psychogios, A., Erwin, A. L., Grebe, T., Retterer, K., & Juusola, J. (2018). de novo missense variants in MEIS2 recapitulate the microdeletion phenotype of cardiac and palate abnormalities, developmental delay, intellectual disability and dysmorphic features. American journal of medical genetics, 176(9), 1845–1851. http://access.bl.uk/ark:/81055/vdc_100069101389.0x00001a