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von Scheibler, E.N.M.M., Bouman, E.S.V., Nuijts, M.A., Bauer, N.J.C., Berendschot, T.T.J.M., Vermeltfoort, P., Bok, L.A., van Eeghen, A.M., Houben, M.L., van Amelsvoort, T.A.M.J., Boot, E., van Egmond-Ebbeling, M.B.
Veröffentlicht in: von Scheibler , E N M M , Bouman , E S V , Nuijts , M A , Bauer , N J C , Berendschot , T T J M , Vermeltfoort , P , Bok , L A , van Eeghen , A M , Houben , M L , van Amelsvoort , T A M J , Boot , E & van Egmond-Ebbeling , M B 2022 , ' Ocular findings in 22q11.2 deletion syndrome: A systematic literature review and results of a Dutch multicenter study ' , American Journal of Medical Genetics Part A , vol. 188 , no. 2 , pp. 569-578 . https://doi.org/10.1002/ajmg.a.62556;
2022
Veröffentlicht in: von Scheibler , E N M M , Bouman , E S V , Nuijts , M A , Bauer , N J C , Berendschot , T T J M , Vermeltfoort , P , Bok , L A , van Eeghen , A M , Houben , M L , van Amelsvoort , T A M J , Boot , E & van Egmond-Ebbeling , M B 2022 , ' Ocular findings in 22q11.2 deletion syndrome: A systematic literature review and results of a Dutch multicenter study ' , American Journal of Medical Genetics Part A , vol. 188 , no. 2 , pp. 569-578 . https://doi.org/10.1002/ajmg.a.62556;
2022