Martin, S., Angolini, E., Audi, J., Bertini, E., Bruno, L. P., Coulter, J., Ferlini, A., Fortunato, F., Frankova, V., Garnier, N., Grauman, Åsa, Gross, E. S., Hauber, B., Hansson, M. G., Kirschner, J., Knieling, F., Kyosovksa, G., Ottombrino, S., Novelli, A., Raming, R., Sansen, S., Saier, C., & Veldwijk, J. [ca. 2024]. Patient preferences in genetic newborn screening for rare diseases: study protocol [Cd]. Freiburg: Universität. https://doi.org/10.1136/bmjopen-2023-081835
ISO-690 (author-date, English)MARTIN, Sylvia, ANGOLINI, Emanuele, AUDI, Jennifer, BERTINI, Enrico, BRUNO, Lucia Pia, COULTER, Joshua, FERLINI, Alessandra, FORTUNATO, Fernanda, FRANKOVA, Vera, GARNIER, Nicolas, GRAUMAN, Åsa, GROSS, Edith Sky, HAUBER, Brett, HANSSON, Mats G, KIRSCHNER, Janbernd, KNIELING, Ferdinand, KYOSOVKSA, Gergana, OTTOMBRINO, Silvia, NOVELLI, Antonio, RAMING, Roman, SANSEN, Stefaan, SAIER, Christina und VELDWIJK, Jorien, 2024. Patient preferences in genetic newborn screening for rare diseases: study protocol. Freiburg: Universität.
Modern Language Association 9th editionMartin, S., E. Angolini, J. Audi, E. Bertini, L. P. Bruno, J. Coulter, A. Ferlini, F. Fortunato, V. Frankova, N. Garnier, Åsa Grauman, E. S. Gross, B. Hauber, M. G. Hansson, J. Kirschner, F. Knieling, G. Kyosovksa, S. Ottombrino, A. Novelli, R. Raming, S. Sansen, C. Saier, und J. Veldwijk. Patient preferences in genetic newborn screening for rare diseases: study protocol. cd, Universität, 2024, https://doi.org/10.1136/bmjopen-2023-081835.
Mohr Siebeck - Recht (Deutsch - Österreich)Martin, Sylvia/Angolini, Emanuele/Audi, Jennifer/Bertini, Enrico/Bruno, Lucia Pia/Coulter, Joshua u. a.: Patient preferences in genetic newborn screening for rare diseases: study protocol, Freiburg 2024.
Emerald - HarvardMartin, S., Angolini, E., Audi, J., Bertini, E., Bruno, L.P., Coulter, J., Ferlini, A., Fortunato, F., Frankova, V., Garnier, N., Grauman, Åsa, Gross, E.S., Hauber, B., Hansson, M.G., Kirschner, J., Knieling, F., Kyosovksa, G., Ottombrino, S., Novelli, A., Raming, R., Sansen, S., Saier, C. und Veldwijk, J. (2024), Patient preferences in genetic newborn screening for rare diseases: study protocol, Bd. , Universität, Freiburg, verfügbar unter:https://doi.org/10.1136/bmjopen-2023-081835.