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L I van den Born

Showing results (11-20 of 18) with videos related to

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Ophthalmic Genetics|June 1, 1994
Thr4Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch familyL I van den Born, M J van Schooneveld, L A de Jong, et al.
Genomics|August 1, 1994
Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease populationS van Soest, L I van den Born, A Gal, et al.
Genomics|November 1, 1992
Evidence for nonallelic genetic heterogeneity in autosomal recessive retinitis pigmentosaL M Bleeker-Wagemakers, A Gal, R Kumar-Singh, et al.
Clinical Genetics|March 1, 1992
Carrier detection in X-linked ocular albinism of the Nettleship-Falls type by DNA analysisA A Bergen, E J Schuurman, L I van den Born, et al.
Journal of Endocrinological Investigation|April 22, 2006
Somatostatin-related therapeutics in ophthalmology: a reviewT Missotten, G S Baarsma, R W A M Kuijpers, et al.
Cytogenetics and Cell Genetics|May 27, 1999
Integrated genetic and physical map of the 1q31-->q32.1 region, encompassing the RP12 locus, the F13B and HF1 genes, and the EEF1AL11 and RPL30 pseudogenesS van Soest, M J van Rossem, J R Heckenlively, et al.
American Journal of Human Genetics|June 5, 2001
Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) geneA I den Hollander, J R Heckenlively, L I van den Born, et al.
Nature Genetics|October 3, 1999
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)A I den Hollander, J B ten Brink, Y J de Kok, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Ophthalmic Genetics|June 1, 1994
Thr4Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch familyL I van den Born, M J van Schooneveld, L A de Jong, et al.
Genomics|August 1, 1994
Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease populationS van Soest, L I van den Born, A Gal, et al.
Genomics|November 1, 1992
Evidence for nonallelic genetic heterogeneity in autosomal recessive retinitis pigmentosaL M Bleeker-Wagemakers, A Gal, R Kumar-Singh, et al.
Clinical Genetics|March 1, 1992
Carrier detection in X-linked ocular albinism of the Nettleship-Falls type by DNA analysisA A Bergen, E J Schuurman, L I van den Born, et al.
Journal of Endocrinological Investigation|April 22, 2006
Somatostatin-related therapeutics in ophthalmology: a reviewT Missotten, G S Baarsma, R W A M Kuijpers, et al.
Cytogenetics and Cell Genetics|May 27, 1999
Integrated genetic and physical map of the 1q31-->q32.1 region, encompassing the RP12 locus, the F13B and HF1 genes, and the EEF1AL11 and RPL30 pseudogenesS van Soest, M J van Rossem, J R Heckenlively, et al.
American Journal of Human Genetics|June 5, 2001
Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) geneA I den Hollander, J R Heckenlively, L I van den Born, et al.
Nature Genetics|October 3, 1999
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)A I den Hollander, J B ten Brink, Y J de Kok, et al.
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