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Showing results (21-30 of 28) with videos related to

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Translational Vision Science & Technology|August 25, 2020
Exome Sequencing in a Swiss Childhood Glaucoma Cohort Reveals <i>CYP1B1</i> and <i>FOXC1</i> Variants as Most Frequent CausesElena Lang, Samuel Koller, Luzy Bähr, et al.
Investigative Ophthalmology & Visual Science|December 17, 2009
Cone versus rod disease in a mutant Rpgr mouse caused by different genetic backgroundsSandra Brunner, Sergej Skosyrski, Renate Kirschner-Schwabe, et al.
Human Molecular Genetics|November 8, 2019
Atonal homolog 7 (ATOH7) loss-of-function mutations in predominant bilateral optic nerve hypoplasiaDavid Atac, Samuel Koller, James V M Hanson, et al.
Biology of Reproduction|June 27, 2008
Overexpression of RPGR leads to male infertility in mice due to defects in flagellar assemblySandra Brunner, Dvora Colman, Alexander J Travis, et al.
Nature Communications|November 22, 2019
Integrin-linked kinase controls retinal angiogenesis and is linked to Wnt signaling and exudative vitreoretinopathyHongryeol Park, Hiroyuki Yamamoto, Lucas Mohn, et al.
Acta Ophthalmologica|September 30, 2020
Genotype-phenotype spectrum in isolated and syndromic nanophthalmosElena Lang, Samuel Koller, David Atac, et al.
JAMA Ophthalmology|May 20, 2021
Genetic Analysis in a Swiss Cohort of Bilateral Congenital CataractDelia Rechsteiner, Lydia Issler, Samuel Koller, et al.
Molecular Vision|June 17, 2008
Identification of novel mutations in X-linked retinitis pigmentosa families and implications for diagnostic testingJohn Neidhardt, Esther Glaus, Birgit Lorenz, et al.
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Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Translational Vision Science & Technology|August 25, 2020
Exome Sequencing in a Swiss Childhood Glaucoma Cohort Reveals <i>CYP1B1</i> and <i>FOXC1</i> Variants as Most Frequent CausesElena Lang, Samuel Koller, Luzy Bähr, et al.
Investigative Ophthalmology & Visual Science|December 17, 2009
Cone versus rod disease in a mutant Rpgr mouse caused by different genetic backgroundsSandra Brunner, Sergej Skosyrski, Renate Kirschner-Schwabe, et al.
Human Molecular Genetics|November 8, 2019
Atonal homolog 7 (ATOH7) loss-of-function mutations in predominant bilateral optic nerve hypoplasiaDavid Atac, Samuel Koller, James V M Hanson, et al.
Biology of Reproduction|June 27, 2008
Overexpression of RPGR leads to male infertility in mice due to defects in flagellar assemblySandra Brunner, Dvora Colman, Alexander J Travis, et al.
Nature Communications|November 22, 2019
Integrin-linked kinase controls retinal angiogenesis and is linked to Wnt signaling and exudative vitreoretinopathyHongryeol Park, Hiroyuki Yamamoto, Lucas Mohn, et al.
Acta Ophthalmologica|September 30, 2020
Genotype-phenotype spectrum in isolated and syndromic nanophthalmosElena Lang, Samuel Koller, David Atac, et al.
JAMA Ophthalmology|May 20, 2021
Genetic Analysis in a Swiss Cohort of Bilateral Congenital CataractDelia Rechsteiner, Lydia Issler, Samuel Koller, et al.
Molecular Vision|June 17, 2008
Identification of novel mutations in X-linked retinitis pigmentosa families and implications for diagnostic testingJohn Neidhardt, Esther Glaus, Birgit Lorenz, et al.
Pageof 3