Identification of a novel compound heterozygous SMG9 variants in a Chinese family with heart and brain malformation syndrome using whole exome sequencing
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1755-8794
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
-
Identification of a novel compound heterozygous SMG9 variants in a Chinese family with heart and brain malformation syndrome using whole exome sequencing ; volume:15 ; number:1 ; day:23 ; month:3 ; year:2022 ; pages:1-8 ; date:12.2022
BMC medical genomics ; 15, Heft 1 (23.3.2022), 1-8, 12.2022
- Urheber
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Yang, Qi
Qin, Zailong
Zhang, Qinle
Yi, Shang
Yi, Sheng
Luo, Jingsi
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1186/s12920-022-01217-9
- URN
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urn:nbn:de:101:1-2022061422061501752958
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:22 MESZ
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Beteiligte
- Yang, Qi
- Qin, Zailong
- Zhang, Qinle
- Yi, Shang
- Yi, Sheng
- Luo, Jingsi
- SpringerLink (Online service)
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