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European Radiology|January 15, 2008
Role of MRI in the management of patients with nephroblastomaJens-Peter Schenk, Norbert Graf, Patrick Günther, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 29, 1998
In vivo fluorescence microscopy of corneal neovascularizationM D Becker, F E Kruse, A M Joussen, et al.
Journal of Medical Genetics|January 16, 1998
An ancestral core haplotype defines the critical region harbouring the North Carolina macular dystrophy gene (MCDR1)C G Sauer, H D Schworm, M Ulbig, et al.
Klinische Monatsblatter Fur Augenheilkunde|December 29, 2005
[Molecular genetic analysis of the BIGH3 gene in lattice type I (Biber-Haab-Dimmer) and granular type II (Avellino) corneal dystrophy: is indirect mutation analysis for hot spots recommended?]C Grünauer-Kloevekorn, S Bräutigam, M Wolter-Roessler, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|April 19, 2013
[Mason's lacing cord. Potential danger of severe open ocular injuries]F Tost, R Großjohann, W Schikorr, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|August 24, 2015
Trends of barriers to eye care among adults with diagnosed diabetes in Germany, 1997-2012S E Baumeister, G Schomerus, R M Andersen, et al.
American Journal of Human Genetics|August 26, 2000
Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophyA Maugeri, B J Klevering, K Rohrschneider, et al.
Klinische Monatsblatter Fur Augenheilkunde|October 26, 2006
[Molecular genetic and histopathological examinations for genotype-phenotype analysis in patients with TGFBI-linked corneal dystrophy]C Grünauer-Kloevekorn, S Braeutigam, E Weidle, et al.
Molecular and Cellular Probes|June 9, 2015
Loss of function of PGAP1 as a cause of severe encephalopathy identified by Whole Exome Sequencing: Lessons of the bioinformatics pipelineM Granzow, N Paramasivam, K Hinderhofer, et al.
The British Journal of Ophthalmology|November 13, 2008
TGFBI (BIGH3) gene mutations in German families: two novel mutations associated with unique clinical and histopathological findingsC Gruenauer-Kloevekorn, I Clausen, E Weidle, et al.
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