Cite
APA Citation
Berg, J., Porteous, M., Reinhardt, D., Gallione, C., Holloway, S., Umasunthar, T., Lux, A., McKinnon, W., Marchuk, D., & Guttmacher, A. (2003). hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations. Journal of medical genetics, 40(8), 585–590. http://access.bl.uk/ark:/81055/vdc_100135134472.0x00003a