1
Vos, Niels, Kleinendorst, Lotte, van der Laan, Liselot, van Uhm, Jorrit, Jansen, Philip R., van Eeghen, Agnies M., Maas, Saskia M., Mannens, Marcel M. A. M., van Haelst, Mieke M.
Veröffentlicht in: Vos , N , Kleinendorst , L , van der Laan , L , van Uhm , J , Jansen , P R , van Eeghen , A M , Maas , S M , Mannens , M M A M & van Haelst , M M 2024 , ' Evaluation of 100 Dutch cases with 16p11.2 deletion and duplication syndromes; from clinical manifestations towards personalized treatment options ' , European Journal of Human Genetics . https://doi.org/10.1038/s41431-024-01601-2;
2024
Veröffentlicht in: Vos , N , Kleinendorst , L , van der Laan , L , van Uhm , J , Jansen , P R , van Eeghen , A M , Maas , S M , Mannens , M M A M & van Haelst , M M 2024 , ' Evaluation of 100 Dutch cases with 16p11.2 deletion and duplication syndromes; from clinical manifestations towards personalized treatment options ' , European Journal of Human Genetics . https://doi.org/10.1038/s41431-024-01601-2;
2024
2
von Scheibler, Emma N. M. M., van der Valk Bouman, Emy S., Nuijts, Myrthe A., Bauer, Noel J. C., Berendschot, Tos T. J. M., Vermeltfoort, Pit, Bok, Levinus A., van Eeghen, Agnies M., Houben, Michiel L., van Amelsvoort, Therese A. M. J., Boot, Erik, van Egmond-Ebbeling, Michelle B.
Veröffentlicht in: von Scheibler , E N M M , van der Valk Bouman , E S , 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 , van der Valk Bouman , E S , 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
3
von Scheibler, Emma N. M. M., van der Valk Bouman, Emy S., Nuijts, Myrthe A., Bauer, Noël J. C., Berendschot, Tos T. J. M., Vermeltfoort, Pit, Bok, Levinus A., van Eeghen, Agnies M., Houben, Michiel L., van Amelsvoort, Thérèse A. M. J., Boot, Erik, van Egmond-Ebbeling, Michelle B.
Veröffentlicht in: von Scheibler , E N M M , van der Valk Bouman , E S , 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 , van der Valk Bouman , E S , 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