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L N Went

Showing results (1-10 of 39) with videos related to

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Human Genetics|January 1, 1985
The genetics of tritan disturbancesL N Went, N Pronk
Documenta Ophthalmologica. Advances in Ophthalmology|September 30, 1982
Leber's optic neuropathy I. Clinical studiesA Stehouwer, L N Went
Annals of Human Genetics|May 1, 1984
Genetic aspects of erythropoietic protoporphyriaL N Went, E C Klasen
Documenta Ophthalmologica. Advances in Ophthalmology|January 1, 1989
Studies on Leber's optic neuropathy IIIA Palan, A Stehouwer, L N Went
Annals of Human Genetics|July 1, 1986
Clinical and genetic studies in six Dutch kindreds with the dysplastic naevus syndromeW Bergman, A Palan, L N Went
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1981
Linkage investigations in two families with hereditary ataxiaJ Van Rossum, H Veenema, L N Went
Human Heredity|January 1, 1978
Frequencies of different types of colour vision defects in the NetherlandsE C Vries-de Mol, L N Went
Journal of the Optical Society of America|November 1, 1981
Color matching in autosomal dominant tritan defectJ Pokorny, V C Smith, L N Went
Journal of the Neurological Sciences|May 1, 1975
An unusual form of spinal muscular atrophy with mental retardation occurring in an inbred populationA Staal, L N Went, H F Busch
Archives of Neurology|January 1, 1985
Familial hypokalemic periodic paralysis. 50-year follow-up of a large familyO J Buruma, G T Bots, L N Went
Pageof 4

Showing results (1-10 of 39) with videos related to

Sort By:
Pageof 4
Human Genetics|January 1, 1985
The genetics of tritan disturbancesL N Went, N Pronk
Documenta Ophthalmologica. Advances in Ophthalmology|September 30, 1982
Leber's optic neuropathy I. Clinical studiesA Stehouwer, L N Went
Annals of Human Genetics|May 1, 1984
Genetic aspects of erythropoietic protoporphyriaL N Went, E C Klasen
Documenta Ophthalmologica. Advances in Ophthalmology|January 1, 1989
Studies on Leber's optic neuropathy IIIA Palan, A Stehouwer, L N Went
Annals of Human Genetics|July 1, 1986
Clinical and genetic studies in six Dutch kindreds with the dysplastic naevus syndromeW Bergman, A Palan, L N Went
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1981
Linkage investigations in two families with hereditary ataxiaJ Van Rossum, H Veenema, L N Went
Human Heredity|January 1, 1978
Frequencies of different types of colour vision defects in the NetherlandsE C Vries-de Mol, L N Went
Journal of the Optical Society of America|November 1, 1981
Color matching in autosomal dominant tritan defectJ Pokorny, V C Smith, L N Went
Journal of the Neurological Sciences|May 1, 1975
An unusual form of spinal muscular atrophy with mental retardation occurring in an inbred populationA Staal, L N Went, H F Busch
Archives of Neurology|January 1, 1985
Familial hypokalemic periodic paralysis. 50-year follow-up of a large familyO J Buruma, G T Bots, L N Went
Pageof 4