Genetic analysis of BRPF1 exon deletion variant causing intellectual developmental disorder with dysmorphic facies and ptosis in a Chinese family
- 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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Genetic analysis of BRPF1 exon deletion variant causing intellectual developmental disorder with dysmorphic facies and ptosis in a Chinese family ; volume:25 ; number:1 ; day:21 ; month:6 ; year:2024 ; pages:1-11 ; date:12.2024
The Egyptian journal of medical human genetics ; 25, Heft 1 (21.6.2024), 1-11, 12.2024
- Urheber
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Liu, Qian
Li, Feifei
Wang, Nana
Fan, Zhengjun
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
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10.1186/s43042-024-00539-w
- URN
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urn:nbn:de:101:1-2409122100102.811708813506
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:38 MESZ
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Beteiligte
- Liu, Qian
- Li, Feifei
- Wang, Nana
- Fan, Zhengjun
- SpringerLink (Online service)
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