- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1750-1172
- Extent
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Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Natural course of pontocerebellar hypoplasia type 2A ; volume:9 ; number:1 ; day:5 ; month:5 ; year:2014 ; pages:1-11 ; date:12.2014
Orphanet journal of rare diseases ; 9, Heft 1 (5.5.2014), 1-11, 12.2014
- Creator
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Sánchez-Albisua, Iciar
- Contributor
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Frölich, Saskia
Barth, Peter G.
Steinlin, Maja
Krägeloh-Mann, Ingeborg
SpringerLink (Online service)
- DOI
-
10.1186/1750-1172-9-70
- URN
-
urn:nbn:de:1111-2016050124416
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 11:00 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
- Sánchez-Albisua, Iciar
- Frölich, Saskia
- Barth, Peter G.
- Steinlin, Maja
- Krägeloh-Mann, Ingeborg
- SpringerLink (Online service)
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Case report: pontocerebellar hypoplasia type 1D
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Human organoid model of pontocerebellar hypoplasia 2a recapitulates brain region-specific size differences
SUNCT and optic nerve hypoplasia
Sternum hypoplasia diagnosed during sternotomy
EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations
Cerebral Artery Hypoplasia among Black Kenyans
Cartilage hair hypoplasia and the RMRP gene
Untersuchungen über die Harnoestrogenausscheidung bei Hypoplasia uteri
Brain morphometry in Pontocerebellar Hypoplasia type 2A
Case report: pontocerebellar hypoplasia type 1D
Brain morphometry in Pontocerebellar Hypoplasia type 2
Pontocerebellar hypoplasia type 2: a neuropathological update
Unilateral cerebellar hypoplasia
Human organoid model of pontocerebellar hypoplasia 2a recapitulates brain region-specific size differences
SUNCT and optic nerve hypoplasia
Sternum hypoplasia diagnosed during sternotomy
EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations
Cerebral Artery Hypoplasia among Black Kenyans
Cartilage hair hypoplasia and the RMRP gene