Description of a patient with developmental delay and dysmorphic features caused by a novel SHANK2 deletion
- 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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Description of a patient with developmental delay and dysmorphic features caused by a novel SHANK2 deletion ; volume:24 ; number:1 ; day:13 ; month:12 ; year:2023 ; pages:1-6 ; date:12.2023
The Egyptian journal of medical human genetics ; 24, Heft 1 (13.12.2023), 1-6, 12.2023
- Urheber
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Molina Herranz, David
Moreno Sánchez, Amelia
Carmen Marcén, Gema
Salinas Salvador, Belén
Pérez Delgado, Raquel
Izquierdo Álvarez, Silvia
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1186/s43042-023-00462-6
- URN
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urn:nbn:de:101:1-2024022810461296255472
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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2025-08-14T10:57:14+0200
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Beteiligte
- Molina Herranz, David
- Moreno Sánchez, Amelia
- Carmen Marcén, Gema
- Salinas Salvador, Belén
- Pérez Delgado, Raquel
- Izquierdo Álvarez, Silvia
- SpringerLink (Online service)
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