Expanding genotype–phenotype correlations in FOXG1 syndrome: results from a patient registry
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource, 1 online resource.
- Sprache
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Englisch
- Erschienen in
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Expanding genotype–phenotype correlations in FOXG1 syndrome: results from a patient registry ; volume:18 ; number:1 ; day:12 ; month:6 ; year:2023 ; pages:1-10 ; date:12.2023
Orphanet journal of rare diseases ; 18, Heft 1 (12.6.2023), 1-10, 12.2023
- Urheber
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Brimble, Elise
Reyes, Kathryn G.
Kuhathaas, Kopika
Devinsky, Orrin
Ruzhnikov, Maura R. Z.
Ortiz-Gonzalez, Xilma R.
Scheffer, Ingrid
Bahi-Buisson, Nadia
Olson, Heather
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1186/s13023-023-02745-y
- URN
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urn:nbn:de:101:1-2023091914115368029912
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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14.08.2025, 10:47 MESZ
Datenpartner
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Beteiligte
- Brimble, Elise
- Reyes, Kathryn G.
- Kuhathaas, Kopika
- Devinsky, Orrin
- Ruzhnikov, Maura R. Z.
- Ortiz-Gonzalez, Xilma R.
- Scheffer, Ingrid
- Bahi-Buisson, Nadia
- Olson, Heather
- SpringerLink (Online service)
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