Evaluation of 100 Dutch cases with 16p11.2 deletion and duplication syndromes; from clinical manifestations towards personalized treatment options
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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Evaluation of 100 Dutch cases with 16p11.2 deletion and duplication syndromes; from clinical manifestations towards personalized treatment options ; volume:32 ; number:11 ; day:11 ; month:4 ; year:2024 ; pages:1387-1401 ; date:11.2024
European journal of human genetics ; 32, Heft 11 (11.4.2024), 1387-1401, 11.2024
- Creator
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Vos, Niels
Kleinendorst, Lotte
Laan, Liselot van der
Uhm, Jorrit van
Jansen, Philip R.
Eeghen, Agnies M. van
Maas, Saskia M.
Mannens, Marcel M.A.M
Haelst, Mieke M. van
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41431-024-01601-2
- URN
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urn:nbn:de:101:1-2502052200308.623207984057
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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05.05.1125, 6:33 AM CET
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Vos, Niels
- Kleinendorst, Lotte
- Laan, Liselot van der
- Uhm, Jorrit van
- Jansen, Philip R.
- Eeghen, Agnies M. van
- Maas, Saskia M.
- Mannens, Marcel M.A.M
- Haelst, Mieke M. van
- SpringerLink (Online service)
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