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B Wissinger

Showing results (21-30 of 61) with videos related to

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Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|October 23, 1998
[Diagnostic error in Leber's optic neuropathy. Value of clinical and molecular genetic studies]B Leo-Kottler, M Christ-Adler, B Wissinger, et al.
Mutation Research|June 19, 2001
Quantitation of heteroplasmy in mitochondrial DNA mutations by primer extension using Vent(R)(exo-) DNA polymerase and RFLP analysisF K Jacobi, J Meyer, C M Pusch, et al.
Cytogenetics and Cell Genetics|January 1, 1997
The two human organic cation transporter genes SLC22A1 and SLC22A2 are located on chromosome 6q26M R Koehler, B Wissinger, V Gorboulev, 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.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|October 2, 2004
[Molecular genetic findings in patients with congenital cone dysfunction. Mutations in the CNGA3, CNGB3, or GNAT2 genes]U Kellner, B Wissinger, S Kohl, et al.
Molecular & General Genetics : MGG|March 20, 1995
RNA editing of a group II intron in Oenothera as a prerequisite for splicingG V Börner, M Mörl, B Wissinger, et al.
German Journal of Ophthalmology|July 1, 1996
Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 geneB Leo-Kottler, M Christ-Adler, B Baumann, et al.
Current Genetics|November 1, 1991
Distribution of RNA editing sites in Oenothera mitochondrial mRNAs and rRNAsW Schuster, R Ternes, V Knoop, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|February 1, 1995
[Correlation between clinical and molecular genetic findings in Leber's optic atrophy]B Leo-Kottler, M Christ-Adler, B Reck, et al.
Acta Anatomica|December 1, 1998
The role of the peripherin/RDS gene in retinal dystrophiesS Kohl, I Giddings, D Besch, et al.
Pageof 7

Showing results (21-30 of 61) with videos related to

Sort By:
Pageof 7
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|October 23, 1998
[Diagnostic error in Leber's optic neuropathy. Value of clinical and molecular genetic studies]B Leo-Kottler, M Christ-Adler, B Wissinger, et al.
Mutation Research|June 19, 2001
Quantitation of heteroplasmy in mitochondrial DNA mutations by primer extension using Vent(R)(exo-) DNA polymerase and RFLP analysisF K Jacobi, J Meyer, C M Pusch, et al.
Cytogenetics and Cell Genetics|January 1, 1997
The two human organic cation transporter genes SLC22A1 and SLC22A2 are located on chromosome 6q26M R Koehler, B Wissinger, V Gorboulev, 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.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|October 2, 2004
[Molecular genetic findings in patients with congenital cone dysfunction. Mutations in the CNGA3, CNGB3, or GNAT2 genes]U Kellner, B Wissinger, S Kohl, et al.
Molecular & General Genetics : MGG|March 20, 1995
RNA editing of a group II intron in Oenothera as a prerequisite for splicingG V Börner, M Mörl, B Wissinger, et al.
German Journal of Ophthalmology|July 1, 1996
Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 geneB Leo-Kottler, M Christ-Adler, B Baumann, et al.
Current Genetics|November 1, 1991
Distribution of RNA editing sites in Oenothera mitochondrial mRNAs and rRNAsW Schuster, R Ternes, V Knoop, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|February 1, 1995
[Correlation between clinical and molecular genetic findings in Leber's optic atrophy]B Leo-Kottler, M Christ-Adler, B Reck, et al.
Acta Anatomica|December 1, 1998
The role of the peripherin/RDS gene in retinal dystrophiesS Kohl, I Giddings, D Besch, et al.
Pageof 7