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N Weisschuh

Showing results (1-10 of 6) with videos related to

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Developments in Ophthalmology|July 25, 2003
Progress in the genetics of glaucomaN Weisschuh, U Schiefer
Clinical Genetics|May 24, 2008
A novel mutation in the FOXC1 gene in a family with Axenfeld-Rieger syndrome and Peters' anomalyN Weisschuh, C Wolf, B Wissinger, et al.
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|March 12, 2008
Morphology of the sella turcica in Axenfeld-Rieger syndrome with PITX2 mutationP Meyer-Marcotty, N Weisschuh, P Dressler, et al.
Molecular & General Genetics : MGG|December 29, 2000
Transcriptional analysis of the gene for glutamine synthetase II and two upstream genes in Streptomyces coelicolor A3(2)N Weisschuh, D Fink, S Vierling, et al.
European Journal of Ophthalmology|May 23, 2023
Clinical characteristics of gyrate atrophy compared with a gyrate atrophy-like retinal phenotypeL Pauleikhoff, N Weisschuh, A Lentzsch, et al.
The British Journal of Ophthalmology|September 20, 2005
Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosaA Schuster, N Weisschuh, H Jägle, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Developments in Ophthalmology|July 25, 2003
Progress in the genetics of glaucomaN Weisschuh, U Schiefer
Clinical Genetics|May 24, 2008
A novel mutation in the FOXC1 gene in a family with Axenfeld-Rieger syndrome and Peters' anomalyN Weisschuh, C Wolf, B Wissinger, et al.
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|March 12, 2008
Morphology of the sella turcica in Axenfeld-Rieger syndrome with PITX2 mutationP Meyer-Marcotty, N Weisschuh, P Dressler, et al.
Molecular & General Genetics : MGG|December 29, 2000
Transcriptional analysis of the gene for glutamine synthetase II and two upstream genes in Streptomyces coelicolor A3(2)N Weisschuh, D Fink, S Vierling, et al.
European Journal of Ophthalmology|May 23, 2023
Clinical characteristics of gyrate atrophy compared with a gyrate atrophy-like retinal phenotypeL Pauleikhoff, N Weisschuh, A Lentzsch, et al.
The British Journal of Ophthalmology|September 20, 2005
Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosaA Schuster, N Weisschuh, H Jägle, et al.
Pageof 1