The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Erschienen in
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In: Journal of Medical Genetics 48.6 (2011): S. 396-406.
- Schlagwort
-
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Gehirn
Zentralnervensystem
- Ereignis
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Veröffentlichung
- (wo)
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Erlangen
- (wer)
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Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
- (wann)
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2011
- Urheber
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Kortüm, Fanny
Das, Soma
Flindt, Max
Morris-Rosendahl, Deborah J.
Stefanova, Irina
Goldstein, Amy
Horn, Denise
Klopocki, Eva
Kluger, Gerhard
Martin, Peter
Rauch, Anita
Roumer, Agathe
Saitta, Sulagna
Walsh, Laurence E.
Wieczorek, Dagmar
Uyanik, Gökhan
Kutsche, Kerstin
Dobyns, William B.
- URN
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urn:nbn:de:bvb:29-opus4-77870
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
25.03.2025, 13:43 MEZ
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Beteiligte
- Kortüm, Fanny
- Das, Soma
- Flindt, Max
- Morris-Rosendahl, Deborah J.
- Stefanova, Irina
- Goldstein, Amy
- Horn, Denise
- Klopocki, Eva
- Kluger, Gerhard
- Martin, Peter
- Rauch, Anita
- Roumer, Agathe
- Saitta, Sulagna
- Walsh, Laurence E.
- Wieczorek, Dagmar
- Uyanik, Gökhan
- Kutsche, Kerstin
- Dobyns, William B.
- Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
Entstanden
- 2011
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