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L I van den Born

Showing results (1-10 of 18) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|July 27, 2006
Acute zonal occult outer retinopathy and multiple sclerosisR Q Hintzen, L I van den Born
Ophthalmic Paediatrics and Genetics|December 1, 1992
A retrospective study of registered retinitis pigmentosa patients in The NetherlandsL I van den Born, A A Bergen, E M Bleeker-Wagemakers
Nederlands Tijdschrift Voor Geneeskunde|November 3, 2005
[From gene to disease; Leber congenital amaurosis (LCA)]S Yzer, L I van den Born, F P M Cremers, et al.
Nederlands Tijdschrift Voor Geneeskunde|December 2, 2021
[New treatment option for Leber hereditary optic neuropathy: early diagnosis is required]Judith A M van Everdingen, Martha Tjon-Fo-Sang, L I van den Born, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 7, 2016
Method for segmentation of the layers in the outer retinaJelena Novosel, Koenraad A Vermeer, Laurence Pierrache, et al.
Clinical Genetics|March 1, 1995
Autosomal recessive retinitis pigmentosa locus maps on chromosome 1q in a large consanguineous family from PakistanJ Leutelt, R Oehlmann, F Younus, et al.
American Journal of Ophthalmology|October 15, 1994
Autosomal recessive retinitis pigmentosa with preserved para-arteriolar retinal pigment epitheliumL I van den Born, S van Soest, M J van Schooneveld, et al.
Ophthalmic Genetics|June 1, 1995
Multipoint linkage analysis and homogeneity tests in 15 Dutch X-linked retinitis pigmentosa familiesA A Bergen, L I Van den Born, E J Schuurman, et al.
Genomics|July 1, 1993
Molecular analysis and genetic mapping of the rhodopsin gene in families with autosomal dominant retinitis pigmentosaS Bunge, H Wedemann, D David, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Fine mapping of the autosomal recessive retinitis pigmentosa locus (RP12) on chromosome 1q; exclusion of the phosducin gene (PDC)S van Soest, S te Nijenhuis, L I van den Born, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Journal of Neurology, Neurosurgery, and Psychiatry|July 27, 2006
Acute zonal occult outer retinopathy and multiple sclerosisR Q Hintzen, L I van den Born
Ophthalmic Paediatrics and Genetics|December 1, 1992
A retrospective study of registered retinitis pigmentosa patients in The NetherlandsL I van den Born, A A Bergen, E M Bleeker-Wagemakers
Nederlands Tijdschrift Voor Geneeskunde|November 3, 2005
[From gene to disease; Leber congenital amaurosis (LCA)]S Yzer, L I van den Born, F P M Cremers, et al.
Nederlands Tijdschrift Voor Geneeskunde|December 2, 2021
[New treatment option for Leber hereditary optic neuropathy: early diagnosis is required]Judith A M van Everdingen, Martha Tjon-Fo-Sang, L I van den Born, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 7, 2016
Method for segmentation of the layers in the outer retinaJelena Novosel, Koenraad A Vermeer, Laurence Pierrache, et al.
Clinical Genetics|March 1, 1995
Autosomal recessive retinitis pigmentosa locus maps on chromosome 1q in a large consanguineous family from PakistanJ Leutelt, R Oehlmann, F Younus, et al.
American Journal of Ophthalmology|October 15, 1994
Autosomal recessive retinitis pigmentosa with preserved para-arteriolar retinal pigment epitheliumL I van den Born, S van Soest, M J van Schooneveld, et al.
Ophthalmic Genetics|June 1, 1995
Multipoint linkage analysis and homogeneity tests in 15 Dutch X-linked retinitis pigmentosa familiesA A Bergen, L I Van den Born, E J Schuurman, et al.
Genomics|July 1, 1993
Molecular analysis and genetic mapping of the rhodopsin gene in families with autosomal dominant retinitis pigmentosaS Bunge, H Wedemann, D David, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Fine mapping of the autosomal recessive retinitis pigmentosa locus (RP12) on chromosome 1q; exclusion of the phosducin gene (PDC)S van Soest, S te Nijenhuis, L I van den Born, et al.
Pageof 2