Berg, J., Porteous, M., Reinhardt, D., Gallione, C., Holloway, S., Umasunthar, T., . . . Guttmacher, A. (2003). Hereditary haemorrhagic telangiectasia: A questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations. BMJ Group.
Trích dẫn kiểu ChicagoBerg, J., et al. Hereditary Haemorrhagic Telangiectasia: A Questionnaire Based Study to Delineate the Different Phenotypes Caused By Endoglin and ALK1 Mutations. BMJ Group, 2003.
Trích dẫn MLABerg, J., et al. Hereditary Haemorrhagic Telangiectasia: A Questionnaire Based Study to Delineate the Different Phenotypes Caused By Endoglin and ALK1 Mutations. BMJ Group, 2003.
Cảnh báo: Các trích dẫn này có thể không phải lúc nào cũng chính xác 100%.