Morphologie, Familienanamnese und Diagnosezeitpunkt bei 26 Patienten mit Axenfeld-Rieger-Syndrom und Glaukom oder okulärer Hypertension
Author:
Publisher
Springer Science and Business Media LLC
Subject
Ophthalmology
Link
http://link.springer.com/content/pdf/10.1007/s00347-006-1335-6.pdf
Reference33 articles.
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2. Borges AS, Susanna R, Carani JC et al. (2002) Genetic analysis of PITX2 and FOXC1 in Rieger Syndrome patients from Brazil. J Glaucoma 11: 51–56
3. Childers NK, Wright JT (1986) Dental and craniofacial anomalies of Axenfeld-Rieger-Syndrome. J Oral Pathology 15: 534–539
4. Emrich RE, Brodie AG, Blayney JR (1965) Prevalence of class I, class II, class III malocclusion in urban population, an epidemiological study. J Dent Res 44: 947–953
5. Espinoza HM, Cox CJ, Semina EV, Amendt BA (2002) A molecular basis for differential developmental anomalies in Axenfeld-Rieger syndrome. Hum Mol Genet (England) 11: 743–753
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