Evaluation of 100 Dutch cases with 16p11.2 deletion and duplication syndromes; from clinical manifestations towards personalized treatment options
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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1 Online-Ressource.
- Sprache
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Englisch
- Erschienen in
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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
- Urheber
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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
- Beteiligte Personen und Organisationen
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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
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:33 MESZ
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Beteiligte
- 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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