Optimal prenatal genetic diagnostic approach for posterior fossa malformation: karyotyping, copy number variant testing, or 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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Optimal prenatal genetic diagnostic approach for posterior fossa malformation: karyotyping, copy number variant testing, or whole-exome sequencing? ; volume:29 ; number:1 ; day:31 ; month:7 ; year:2024 ; pages:1-9 ; date:12.2024
European journal of medical research ; 29, Heft 1 (31.7.2024), 1-9, 12.2024
- Urheber
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Juan, Zhang
Cuixia, Guo
Yuanjie, Cui
Yan, Liu
Ling, Yao
Tiejuan, Zhang
Li, Wang
Jijing, Han
Guohui, Zhang
Yousheng, Yan
Qingqing, Wu
Lijuan, Sun
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1186/s40001-024-01993-3
- URN
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urn:nbn:de:101:1-2410250851131.463259906994
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:34 MESZ
Datenpartner
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Beteiligte
- Juan, Zhang
- Cuixia, Guo
- Yuanjie, Cui
- Yan, Liu
- Ling, Yao
- Tiejuan, Zhang
- Li, Wang
- Jijing, Han
- Guohui, Zhang
- Yousheng, Yan
- Qingqing, Wu
- Lijuan, Sun
- SpringerLink (Online service)
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