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Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|June 5, 2009
[Genetics of Usher syndrome]H J BolzKlinische Monatsblatter Fur Augenheilkunde|March 30, 2017
[Next-Generation Sequencing: A Quantum Leap in Ophthalmology Research and Diagnostics]H J BolzDer Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|July 29, 2018
[Genetic diagnostics of retinal dystrophies : Breakthrough with new methods of DNA sequencing]H J BolzKlinische Monatsblatter Fur Augenheilkunde|March 4, 2017
[Segregation Analysis in Inherited Eye Disorders: An Academic Add-on or An Essential Effort?]M N Preising, H J BolzDer Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|December 6, 2014
[Genetics of congenital aniridia]C Neuhaus, C Betz, C Bergmann, et al.Klinische Monatsblatter Fur Augenheilkunde|March 30, 2017
[Genotype-Phenotype Correlations in Patients with CRB1 Mutations]C Papadopoulou Laiou, M N Preising, H J Bolz, et al.Clinical Genetics|April 4, 2017
Genome-wide linkage and sequence analysis challenge CCDC66 as a human retinal dystrophy candidate gene and support a distinct NMNAT1-related fundus phenotypeA O Khan, B S Budde, P Nürnberg, et al.The British Journal of Ophthalmology|May 1, 2009
Characterisation of severe rod-cone dystrophy in a consanguineous family with a splice site mutation in the MERTK geneP Charbel Issa, H J Bolz, I Ebermann, et al.Clinical Genetics|November 4, 2016
Extension of the clinical and molecular phenotype of DIAPH1-associated autosomal dominant hearing loss (DFNA1)C Neuhaus, R Lang-Roth, U Zimmermann, et al.Journal of Medical Genetics|April 10, 2009
GPR98 mutations cause Usher syndrome type 2 in malesI Ebermann, M H J Wiesen, E Zrenner, et al.Pageof 1