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T P Dryja

Showing results (81-90 of 141) with videos related to

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American Journal of Human Genetics|June 1, 1993
Molecular etiology of low-penetrance retinoblastoma in two pedigreesT P Dryja, J Rapaport, T L McGee, et al.
Nature Genetics|June 16, 1999
Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatusH Yamamoto, A Simon, U Eriksson, et al.
American Journal of Ophthalmology|August 15, 1985
Linkage between the X-linked retinitis pigmentosa locus and the L1.28 locusS Mukai, T P Dryja, G A Bruns, et al.
Experimental Eye Research|August 10, 2000
Evaluation of the myosin VIIA gene and visual function in patients with Usher syndrome type IA K Bharadwaj, J P Kasztejna, S Huq, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 1995
Constitutive activation of phototransduction by K296E opsin is not a cause of photoreceptor degenerationT Li, W K Franson, J W Gordon, et al.
American Journal of Ophthalmology|May 15, 1991
Ocular findings in patients with autosomal dominant retinitis pigmentosa and rhodopsin, proline-347-leucineE L Berson, B Rosner, M A Sandberg, et al.
American Journal of Ophthalmology|June 1, 1984
Linkage of genes for human esterase D and hereditary retinoblastomaS Mukai, J M Rapaport, J A Shields, et al.
Investigative Ophthalmology & Visual Science|September 1, 1982
Mass cultivation of bovine ocular pigment epithelial cells in microcarrier suspension cultureD J D'Amico, T P Dryja, M A Tyo, et al.
Cancer Genetics and Cytogenetics|December 1, 1984
Isolation of human chromosome 13-specific DNA sequences cloned from flow sorted chromosomes and potentially linked to the retinoblastoma locusM Lalande, T P Dryja, R R Schreck, et al.
Retina (Philadelphia, Pa.)|January 1, 1983
Isolation of DNA fragments from chromosome 13T P Dryja, G A Bruns, S H Orkin, et al.
Pageof 15

Showing results (81-90 of 141) with videos related to

Sort By:
Pageof 15
American Journal of Human Genetics|June 1, 1993
Molecular etiology of low-penetrance retinoblastoma in two pedigreesT P Dryja, J Rapaport, T L McGee, et al.
Nature Genetics|June 16, 1999
Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatusH Yamamoto, A Simon, U Eriksson, et al.
American Journal of Ophthalmology|August 15, 1985
Linkage between the X-linked retinitis pigmentosa locus and the L1.28 locusS Mukai, T P Dryja, G A Bruns, et al.
Experimental Eye Research|August 10, 2000
Evaluation of the myosin VIIA gene and visual function in patients with Usher syndrome type IA K Bharadwaj, J P Kasztejna, S Huq, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 1995
Constitutive activation of phototransduction by K296E opsin is not a cause of photoreceptor degenerationT Li, W K Franson, J W Gordon, et al.
American Journal of Ophthalmology|May 15, 1991
Ocular findings in patients with autosomal dominant retinitis pigmentosa and rhodopsin, proline-347-leucineE L Berson, B Rosner, M A Sandberg, et al.
American Journal of Ophthalmology|June 1, 1984
Linkage of genes for human esterase D and hereditary retinoblastomaS Mukai, J M Rapaport, J A Shields, et al.
Investigative Ophthalmology & Visual Science|September 1, 1982
Mass cultivation of bovine ocular pigment epithelial cells in microcarrier suspension cultureD J D'Amico, T P Dryja, M A Tyo, et al.
Cancer Genetics and Cytogenetics|December 1, 1984
Isolation of human chromosome 13-specific DNA sequences cloned from flow sorted chromosomes and potentially linked to the retinoblastoma locusM Lalande, T P Dryja, R R Schreck, et al.
Retina (Philadelphia, Pa.)|January 1, 1983
Isolation of DNA fragments from chromosome 13T P Dryja, G A Bruns, S H Orkin, et al.
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