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L N Went

Showing results (21-30 of 39) with videos related to

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Journal of the Neurological Sciences|November 1, 1992
Hereditary spastic dystonia with Leber's hereditary optic neuropathy: neuropathological findingsG W Bruyn, G T Bots, L N Went, et al.
Journal of Medical Genetics|May 1, 1992
X linked progressive cone dystrophy with specific attention to carrier detectionJ A van Everdingen, L N Went, J E Keunen, et al.
Journal of Medical Genetics|March 1, 1975
A family with apparently sex-linked optic atrophyL N Went, E C De Vries-De Mol, H J Völker-Dieben
Documenta Ophthalmologica. Advances in Ophthalmology|September 30, 1982
Leber's optic neuropathy II. Fluorescein angiographic studiesA Stehouwer, J A Oosterhuis, A H Renger-van Dijk, et al.
Journal of the Neurological Sciences|September 1, 1988
Oculomotor defects in patients with Huntington's disease and their offspringH Collewijn, L N Went, E P Tamminga, et al.
Hemoglobin|January 1, 1977
Binding of Protoporphyrin to hemoglobin in red blood cells of patients with erythropoietic protoporphyriaJ van Steveninck, T M Dubbelman, A F de Goeij, et al.
Annals of Human Genetics|July 1, 1983
Huntington's Chorea in the Netherlands. The problem of genetic heterogeneityL N Went, M Vegter-van der Vlis, G W Bruyn, et al.
Human Genetics|September 1, 1988
Further evidence for localization of the gene of erythrokeratodermia variabilisJ G van der Schroeff, I van Leeuwen-Cornelisse, A van Haeringen, et al.
Journal of the Neurological Sciences|July 1, 1988
Hereditary cerebral haemorrhage caused by cortical amyloid angiopathyW Luyendijk, G T Bots, M Vegter-van der Vlis, et al.
American Journal of Human Genetics|March 1, 1992
Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsinC J Weitz, Y Miyake, K Shinzato, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
Journal of the Neurological Sciences|November 1, 1992
Hereditary spastic dystonia with Leber's hereditary optic neuropathy: neuropathological findingsG W Bruyn, G T Bots, L N Went, et al.
Journal of Medical Genetics|May 1, 1992
X linked progressive cone dystrophy with specific attention to carrier detectionJ A van Everdingen, L N Went, J E Keunen, et al.
Journal of Medical Genetics|March 1, 1975
A family with apparently sex-linked optic atrophyL N Went, E C De Vries-De Mol, H J Völker-Dieben
Documenta Ophthalmologica. Advances in Ophthalmology|September 30, 1982
Leber's optic neuropathy II. Fluorescein angiographic studiesA Stehouwer, J A Oosterhuis, A H Renger-van Dijk, et al.
Journal of the Neurological Sciences|September 1, 1988
Oculomotor defects in patients with Huntington's disease and their offspringH Collewijn, L N Went, E P Tamminga, et al.
Hemoglobin|January 1, 1977
Binding of Protoporphyrin to hemoglobin in red blood cells of patients with erythropoietic protoporphyriaJ van Steveninck, T M Dubbelman, A F de Goeij, et al.
Annals of Human Genetics|July 1, 1983
Huntington's Chorea in the Netherlands. The problem of genetic heterogeneityL N Went, M Vegter-van der Vlis, G W Bruyn, et al.
Human Genetics|September 1, 1988
Further evidence for localization of the gene of erythrokeratodermia variabilisJ G van der Schroeff, I van Leeuwen-Cornelisse, A van Haeringen, et al.
Journal of the Neurological Sciences|July 1, 1988
Hereditary cerebral haemorrhage caused by cortical amyloid angiopathyW Luyendijk, G T Bots, M Vegter-van der Vlis, et al.
American Journal of Human Genetics|March 1, 1992
Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsinC J Weitz, Y Miyake, K Shinzato, et al.
Pageof 4