Showing results (1-10 of 13) with videos related to
Sort By:
Pageof 2
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 20, 2005
[Best's disease. Overview of pathology and its causes]B Lorenz, M N PreisingDer Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|June 10, 2010
[Genetics of neuronal ceroidlipofuscinoses. Aspects of genetic counseling]M N Preising, B LorenzDer Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|April 4, 2009
[Genetic diseases of the retinal pigment epithelium]M N Preising, B LorenzKlinische Monatsblatter Fur Augenheilkunde|March 25, 2016
[Albinism and the Range of Fundus Hypopigmentation, Macular Hypoplasia, and Nystagmus]M N Preising, B LorenzKlinische 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 BolzKlinische Monatsblatter Fur Augenheilkunde|October 30, 2015
[Recruitment of Suitable Families to Identify Causative Genes in Hereditary Strabismus]M N Preising, P H T Steinmüller, B LorenzBiomed Research International|September 7, 2018
Unexpected Genetic Cause in Two Female Siblings with High Myopia and Reduced Visual AcuityM N Preising, C Friedburg, W Bowl, et al.Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|May 26, 2007
[Genetic and clinical heterogeneity in LCA patients. The end of uniformity]M N Preising, K Paunescu, C Friedburg, 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.Ophthalmology|February 27, 2007
Genotype-phenotype correlation in a German family with a novel complex CRX mutation extending the open reading frameK Paunescu, M N Preising, B Janke, et al.Pageof 2