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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