Phenotypic and genetic analysis of children with unexplained neurodevelopmental delay and neurodevelopmental comorbidities in a Chinese cohort using trio-based whole-exome sequencing
- 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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Phenotypic and genetic analysis of children with unexplained neurodevelopmental delay and neurodevelopmental comorbidities in a Chinese cohort using trio-based whole-exome sequencing ; volume:19 ; number:1 ; day:19 ; month:5 ; year:2024 ; pages:1-17 ; date:12.2024
Orphanet journal of rare diseases ; 19, Heft 1 (19.5.2024), 1-17, 12.2024
- Creator
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Wu, Ruohao
Li, Xiaojuan
Meng, Zhe
Li, Pinggan
He, Zhanwen
Liang, Liyang
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s13023-024-03214-w
- URN
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urn:nbn:de:101:1-2407291141163.935386803185
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:50 AM CEST
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
- Wu, Ruohao
- Li, Xiaojuan
- Meng, Zhe
- Li, Pinggan
- He, Zhanwen
- Liang, Liyang
- SpringerLink (Online service)
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