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. und Veldwijk, J. (2024) Patient preferences in genetic newborn screening for rare diseases: study protocol [cd]. Freiburg: Universität. doi:10.1136/bmjopen-2023-081835.

Martin, Sylvia, Emanuele Angolini, Jennifer Audi, Enrico Bertini, Lucia Pia Bruno, Joshua Coulter, Alessandra Ferlini, Fernanda Fortunato, Vera Frankova, Nicolas Garnier, Åsa Grauman, Edith Sky Gross, Brett Hauber, Mats G Hansson, Janbernd Kirschner, Ferdinand Knieling, Gergana Kyosovksa, Silvia Ottombrino, Antonio Novelli, Roman Raming, Stefaan Sansen, Christina Saier, und Jorien Veldwijk. Patient preferences in genetic newborn screening for rare diseases: study protocol. Cd. Freiburg: Universität, [2024?], Freiburg: Universität, [2024?]. https://doi.org/10.1136/bmjopen-2023-081835.

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]. Universität. https://doi.org/10.1136/bmjopen-2023-081835

Martin, 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.

MARTIN, Sylvia, Emanuele ANGOLINI, Jennifer AUDI, Enrico BERTINI, Lucia Pia BRUNO, Joshua COULTER, Alessandra FERLINI, Fernanda FORTUNATO, Vera FRANKOVA, Nicolas GARNIER, Åsa GRAUMAN, Edith Sky GROSS, Brett HAUBER, Mats G HANSSON, Janbernd KIRSCHNER, Ferdinand KNIELING, Gergana KYOSOVKSA, Silvia OTTOMBRINO, Antonio NOVELLI, Roman RAMING, Stefaan SANSEN, Christina SAIER und Jorien VELDWIJK, 2024. Patient preferences in genetic newborn screening for rare diseases: study protocol. Freiburg: Universität