Correction to: First observation of secondary childhood glaucoma in Coffin-Siris syndrome: a case report and literature review
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2415
- 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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Correction to: First observation of secondary childhood glaucoma in Coffin-Siris syndrome: a case report and literature review ; volume:21 ; number:1 ; day:22 ; month:1 ; year:2021 ; pages:1 ; date:12.2021
BMC ophthalmology ; 21, Heft 1 (22.1.2021), 1, 12.2021
- Creator
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Diel, Heidi
Ding, Can
Grehn, Franz
Chronopoulos, Panagiotis
Bartsch, Oliver
Hoffmann, Esther M.
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s12886-021-01821-w
- URN
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urn:nbn:de:101:1-2021031419072430557714
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:27 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
- Diel, Heidi
- Ding, Can
- Grehn, Franz
- Chronopoulos, Panagiotis
- Bartsch, Oliver
- Hoffmann, Esther M.
- SpringerLink (Online service)
Other Objects (12)
First observation of secondary childhood glaucoma in Coffin-Siris syndrome: a case report and literature review
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Coffin-Siris syndrome with Mayer-Rokitansky-Küster-Hauser syndrome: a case report
The missing link: ARID1B non-truncating variants causing Coffin-Siris syndrome due to protein aggregation
Entwicklung des Phänotyps vom Kind zum Erwachsenen bei Menschen mit seltenen Syndromen: das Coffin-Siris-Syndrom
Mutations in SMARCB1 and in other Coffin–Siris syndrome genes lead to various brain midline defects
A rare Coffin-Siris syndrome induced by SOX11: a de novo nonsense variant of short stature
Coffin, Geraldine
Short stature and melanocytic nevi in a girl with ARID1B-related Coffin-Siris syndrome: a case report
The overlapping of phenotypes in Wiedemann-Steiner, Kleefstra and Coffin-Siris syndromes: a study of eleven patients
Siris
First observation of secondary childhood glaucoma in Coffin-Siris syndrome: a case report and literature review
Das Coffin-Siris-Syndrom
Klinische und genetische Analyse von 22 Patienten mit Coffin-Siris-Syndrom
Coffin-Siris syndrome with Mayer-Rokitansky-Küster-Hauser syndrome: a case report
The missing link: ARID1B non-truncating variants causing Coffin-Siris syndrome due to protein aggregation
Entwicklung des Phänotyps vom Kind zum Erwachsenen bei Menschen mit seltenen Syndromen: das Coffin-Siris-Syndrom
Mutations in SMARCB1 and in other Coffin–Siris syndrome genes lead to various brain midline defects
A rare Coffin-Siris syndrome induced by SOX11: a de novo nonsense variant of short stature
Coffin, Geraldine
Short stature and melanocytic nevi in a girl with ARID1B-related Coffin-Siris syndrome: a case report
The overlapping of phenotypes in Wiedemann-Steiner, Kleefstra and Coffin-Siris syndromes: a study of eleven patients
Siris
First observation of secondary childhood glaucoma in Coffin-Siris syndrome: a case report and literature review
Das Coffin-Siris-Syndrom
Klinische und genetische Analyse von 22 Patienten mit Coffin-Siris-Syndrom
Coffin-Siris syndrome with Mayer-Rokitansky-Küster-Hauser syndrome: a case report
The missing link: ARID1B non-truncating variants causing Coffin-Siris syndrome due to protein aggregation
Entwicklung des Phänotyps vom Kind zum Erwachsenen bei Menschen mit seltenen Syndromen: das Coffin-Siris-Syndrom
Mutations in SMARCB1 and in other Coffin–Siris syndrome genes lead to various brain midline defects
A rare Coffin-Siris syndrome induced by SOX11: a de novo nonsense variant of short stature
Coffin, Geraldine
Short stature and melanocytic nevi in a girl with ARID1B-related Coffin-Siris syndrome: a case report
The overlapping of phenotypes in Wiedemann-Steiner, Kleefstra and Coffin-Siris syndromes: a study of eleven patients