Optimal prenatal genetic diagnostic approach for posterior fossa malformation: karyotyping, copy number variant testing, or whole-exome sequencing?

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: 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

Creator: Juan, Zhang
Cuixia, Guo
Yuanjie, Cui
Yan, Liu
Ling, Yao
Tiejuan, Zhang
Li, Wang
Jijing, Han
Guohui, Zhang
Yousheng, Yan
Qingqing, Wu
Lijuan, Sun

Contributor: SpringerLink (Online service)

DOI: 10.1186/s40001-024-01993-3

URN: urn:nbn:de:101:1-2410250851131.463259906994

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 17.09.2025, 2:32 PM CEST

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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
SpringerLink (Online service)

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Optimal prenatal genetic diagnostic approach for posterior fossa malformation: karyotyping, copy number variant testing, or whole-exome sequencing?

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Other Objects (12)

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