Cite

    Dreßen, M., Lahm, H., Lahm, A., Wolf, K., Doppler, S., Deutsch, M., Cleuziou, J., Pabst von Ohain, J., Schön, P., Ewert, P., Malcic, I., Lange, R., & Krane, M. (2016). a novel de novo TBX5 mutation in a patient with Holt–Oram syndrome leading to a dramatically reduced biological function. Molecular genetics & genomic medicine, 4(5), 557–567. http://access.bl.uk/ark:/81055/vdc_100036424591.0x000001