Identifying rare genetic variants in 21 highly multiplex autism families: the role of diagnosis and autistic traits
- 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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Identifying rare genetic variants in 21 highly multiplex autism families: the role of diagnosis and autistic traits ; volume:28 ; number:5 ; day:26 ; month:1 ; year:2023 ; pages:2148-2157 ; date:5.2023
Molecular psychiatry ; 28, Heft 5 (26.1.2023), 2148-2157, 5.2023
- Urheber
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More, Ravi Prabhakar
Warrier, Varun
Brunel, Helena
Buckingham, Clara
Smith, Paula
Allison, Carrie
Holt, Rosemary
Bradshaw, Charles R.
Baron-Cohen, Simon
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1038/s41380-022-01938-4
- URN
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urn:nbn:de:101:1-2024010308341838911969
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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25.12.2025, 15:27 MEZ
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Beteiligte
- More, Ravi Prabhakar
- Warrier, Varun
- Brunel, Helena
- Buckingham, Clara
- Smith, Paula
- Allison, Carrie
- Holt, Rosemary
- Bradshaw, Charles R.
- Baron-Cohen, Simon
- SpringerLink (Online service)
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