Search research articles
Contact Us
Filters
Showing results (11-20 of 18) with videos related to
Page
of 2
Sort By:
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 family
L 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 population
S van Soest, L I van den Born, A Gal, et al.
Genomics
|
November 1, 1992
Evidence for nonallelic genetic heterogeneity in autosomal recessive retinitis pigmentosa
L 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 analysis
A 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 review
T 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 pseudogenes
S 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) gene
A 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.
Page
of 2
Search research articles
Search
Showing results (11-20 of 18) with videos related to
Sort By:
Page
of 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 family
L 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 population
S van Soest, L I van den Born, A Gal, et al.
Genomics
|
November 1, 1992
Evidence for nonallelic genetic heterogeneity in autosomal recessive retinitis pigmentosa
L 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 analysis
A 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 review
T 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 pseudogenes
S 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) gene
A 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.
Page
of 2