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A J Pinckers

Showing results (41-50 of 55) with videos related to

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Human Genetics|March 10, 1999
Refined mapping of the gene for autosomal dominant retinitis pigmentosa (RP17) on chromosome 17q22A I den Hollander, S D van der Velde-Visser, A J Pinckers, 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.
Ophthalmology|July 27, 2001
Null mutation in the human 11-cis retinol dehydrogenase gene associated with fundus albipunctatusC A Driessen, B P Janssen, H J Winkens, et al.
American Journal of Human Genetics|October 1, 1990
Deletions in patients with classical choroideremia vary in size from 45 kb to several megabasesF P Cremers, E M Sankila, F Brunsmann, et al.
Human Genetics|December 1, 1991
Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls typeA A Bergen, C Samanns, E J Schuurman, et al.
Human Molecular Genetics|July 1, 1996
Positional cloning of the gene for X-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1R Roepman, G van Duijnhoven, T Rosenberg, et al.
American Journal of Medical Genetics|June 5, 1995
Carrier detection of Batten disease (juvenile neuronal ceroid-lipofuscinosis)P E Taschner, N de Vos, J G Post, et al.
Brain : a Journal of Neurology|October 1, 1991
Myotonic dystrophy. Predictive value of normal results on clinical examinationH G Brunner, H J Smeets, W Nillesen, et al.
American Journal of Human Genetics|June 1, 1992
Detection and characterization of point mutations in the choroideremia candidate gene by PCR-SSCP analysis and direct DNA sequencingJ A van den Hurk, T J van de Pol, C M Molloy, et al.
Neuropediatrics|August 1, 1982
Peripheral and central myelinopathy in Cockayne's syndrome. Report of 3 siblingsM G Smits, F J Gabreëls, W O Renier, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
Human Genetics|March 10, 1999
Refined mapping of the gene for autosomal dominant retinitis pigmentosa (RP17) on chromosome 17q22A I den Hollander, S D van der Velde-Visser, A J Pinckers, 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.
Ophthalmology|July 27, 2001
Null mutation in the human 11-cis retinol dehydrogenase gene associated with fundus albipunctatusC A Driessen, B P Janssen, H J Winkens, et al.
American Journal of Human Genetics|October 1, 1990
Deletions in patients with classical choroideremia vary in size from 45 kb to several megabasesF P Cremers, E M Sankila, F Brunsmann, et al.
Human Genetics|December 1, 1991
Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls typeA A Bergen, C Samanns, E J Schuurman, et al.
Human Molecular Genetics|July 1, 1996
Positional cloning of the gene for X-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1R Roepman, G van Duijnhoven, T Rosenberg, et al.
American Journal of Medical Genetics|June 5, 1995
Carrier detection of Batten disease (juvenile neuronal ceroid-lipofuscinosis)P E Taschner, N de Vos, J G Post, et al.
Brain : a Journal of Neurology|October 1, 1991
Myotonic dystrophy. Predictive value of normal results on clinical examinationH G Brunner, H J Smeets, W Nillesen, et al.
American Journal of Human Genetics|June 1, 1992
Detection and characterization of point mutations in the choroideremia candidate gene by PCR-SSCP analysis and direct DNA sequencingJ A van den Hurk, T J van de Pol, C M Molloy, et al.
Neuropediatrics|August 1, 1982
Peripheral and central myelinopathy in Cockayne's syndrome. Report of 3 siblingsM G Smits, F J Gabreëls, W O Renier, et al.
Pageof 6