Klippel-Feil syndrome with multiple skeletal anomalies, Dandy-Walker spectrum, and occipital cephalocele—a rare presentation
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2090-4762
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Klippel-Feil syndrome with multiple skeletal anomalies, Dandy-Walker spectrum, and occipital cephalocele—a rare presentation ; volume:52 ; number:1 ; day:7 ; month:1 ; year:2021 ; pages:1-7 ; date:12.2021
The Egyptian Journal of Radiology and Nuclear Medicine ; 52, Heft 1 (7.1.2021), 1-7, 12.2021
- Creator
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Shoaib, Mohammad
Swarup, M. Sarthak
Pradhan, Gaurav
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s43055-020-00402-z
- URN
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urn:nbn:de:101:1-2021020809132491081357
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:22 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Shoaib, Mohammad
- Swarup, M. Sarthak
- Pradhan, Gaurav
- SpringerLink (Online service)
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Das Klippel-Feil-Syndrom
Untersuchung zur Erblichkeit des Klippel-Feil'-Syndroms
Das sogenannte Klippel-Feil-Syndrom - Klinik, Pathogenese, Vererbung
“Clinical triad” findings in pediatric Klippel-Feil patients
The predictive ability of occipital to C3 angle for dysphagia after occipitocervical fusion in patients with combined C2–3 Klippel-Feil syndrome
Atlasassimilation kombiniert mit Klippel-Feil-Syndrom : Bericht e. Falles
Halswirbelkörper-Synostosen, Klippel-Feil-Syndrom: Wiederholungsrisiko für Kinder und Geschwister
Mutation in MEOX1gene causes a recessive Klippel-Feil syndrome subtype
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