Prenatal diagnosis and molecular cytogenetic analyses of a paternal inherited deletion of 1q23.3 encompassing PBX1 gene
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1755-8166
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Prenatal diagnosis and molecular cytogenetic analyses of a paternal inherited deletion of 1q23.3 encompassing PBX1 gene ; volume:15 ; number:1 ; day:21 ; month:12 ; year:2022 ; pages:1-5 ; date:12.2022
Molecular cytogenetics ; 15, Heft 1 (21.12.2022), 1-5, 12.2022
- Urheber
-
Luo, Man
Gu, Xia
Zhou, Ting
Chen, Chaoli
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s13039-022-00632-y
- URN
-
urn:nbn:de:101:1-2023030321004302825909
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
- 14.08.2025, 08:52 UTC
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Beteiligte
- Luo, Man
- Gu, Xia
- Zhou, Ting
- Chen, Chaoli
- SpringerLink (Online service)
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