Joanna van Wijk

DR.

20022019
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Research Output 2002 2019

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Comment/Letter to the editor
2017

Erratum: Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations (The American Journal of Human Genetics (2017) 101(5) (789–802) (S0002929717303877) (10.1016/j.ajhg.2017.09.018))

Sanna-Cherchi, S., Khan, K., Westland, R., Krithivasan, P., Fievet, L., Rasouly, H. M., Ionita-Laza, I., Capone, V. P., Fasel, D. A., Kiryluk, K., Kamalakaran, S., Bodria, M., Otto, E. A., Sampson, M. G., Gillies, C. E., Vega-Warner, V., Vukojevic, K., Pediaditakis, I., Makar, G. S., Mitrotti, A. & 29 othersVerbitsky, M., Martino, J., Liu, Q., Na, Y. J., Goj, V., Ardissino, G., Gigante, M., Gesualdo, L., Janezcko, M., Zaniew, M., Mendelsohn, C. L., Shril, S., Hildebrandt, F., van Wijk, J. A. E., Arapovic, A., Saraga, M., Allegri, L., Izzi, C., Scolari, F., Tasic, V., Ghiggeri, G. M., Latos-Bielenska, A., Materna-Kiryluk, A., Mane, S., Goldstein, D. B., Lifton, R. P., Katsanis, N., Davis, E. E. & Gharavi, A. G., 7 Dec 2017, In : American journal of human genetics. 101, 6, p. 1034 1 p.

Research output: Contribution to journalComment/Letter to the editorAcademic