Expanding genotype–phenotype correlations in FOXG1 syndrome: results from a patient registry
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource, 1 online resource.
- Language
-
Englisch
- Bibliographic citation
-
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
- Creator
-
Brimble, Elise
Reyes, Kathryn G.
Kuhathaas, Kopika
Devinsky, Orrin
Ruzhnikov, Maura R. Z.
Ortiz-Gonzalez, Xilma R.
Scheffer, Ingrid
Bahi-Buisson, Nadia
Olson, Heather
- Contributor
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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
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:47 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- 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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