Cite

    Lin, A. E., Michot, C., Cormier‐Daire, V., L'Ecuyer, T. J., Matherne, G. P., Barnes, B. H., Humberson, J. B., Edmondson, A. C., Zackai, E., O'Connor, M. J., Kaplan, J. D., Ebeid, M. R., Krier, J., Krieg, E., Ghoshhajra, B., & Lindsay, M. E. (2016). gain‐of‐function mutations in SMAD4 cause a distinctive repertoire of cardiovascular phenotypes in patients with Myhre syndrome. American journal of medical genetics, 170(10), 2617–2631. http://access.bl.uk/ark:/81055/vdc_100036362786.0x00000f