Phenotypic and genetic analysis of children with unexplained neurodevelopmental delay and neurodevelopmental comorbidities in a Chinese cohort using trio-based whole-exome sequencing
- 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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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
- Urheber
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Wu, Ruohao
Li, Xiaojuan
Meng, Zhe
Li, Pinggan
He, Zhanwen
Liang, Liyang
- Beteiligte Personen und Organisationen
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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
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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14.08.2025, 10:50 MESZ
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Beteiligte
- Wu, Ruohao
- Li, Xiaojuan
- Meng, Zhe
- Li, Pinggan
- He, Zhanwen
- Liang, Liyang
- SpringerLink (Online service)
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