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T P Dryja

Showing results (111-120 of 141) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|October 24, 1995
Mutations in the gene encoding the alpha subunit of the rod cGMP-gated channel in autosomal recessive retinitis pigmentosaT P Dryja, J T Finn, Y W Peng, et al.
American Journal of Human Genetics|January 1, 1986
Chromosome 13 homozygosity in osteosarcoma without retinoblastomaT P Dryja, J M Rapaport, J Epstein, et al.
Nature Genetics|June 1, 1992
A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosaP J Rosenfeld, G S Cowley, T L McGee, et al.
Experimental Eye Research|May 1, 1985
Glial cell component in retinoblastomaJ L Craft, D N Sang, T P Dryja, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 1, 1985
Accuracy of detection of the retinoblastoma gene by esterase D linkageS L Halloran, J A Boughman, T P Dryja, et al.
Investigative Ophthalmology & Visual Science|April 1, 1994
In vivo transfer of a reporter gene to the retina mediated by an adenoviral vectorT Li, M Adamian, D J Roof, et al.
Genomics|September 1, 1993
Complete genomic sequence of the human retinoblastoma susceptibility geneJ Toguchida, T L McGee, J C Paterson, et al.
Nature|October 16, 1986
A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcomaS H Friend, R Bernards, S Rogelj, et al.
Ophthalmology|September 15, 1999
Intraocular-central nervous system lymphoma: clinical features, diagnosis, and outcomesE K Akpek, I Ahmed, F H Hochberg, et al.
Investigative Ophthalmology & Visual Science|August 1, 1990
Analysis of genes coding for S-antigen, interstitial retinol binding protein, and the alpha-subunit of cone transducin in patients with retinitis pigmentosaP J Ringens, M Fang, T Shinohara, et al.
Pageof 15

Showing results (111-120 of 141) with videos related to

Sort By:
Pageof 15
Proceedings of the National Academy of Sciences of the United States of America|October 24, 1995
Mutations in the gene encoding the alpha subunit of the rod cGMP-gated channel in autosomal recessive retinitis pigmentosaT P Dryja, J T Finn, Y W Peng, et al.
American Journal of Human Genetics|January 1, 1986
Chromosome 13 homozygosity in osteosarcoma without retinoblastomaT P Dryja, J M Rapaport, J Epstein, et al.
Nature Genetics|June 1, 1992
A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosaP J Rosenfeld, G S Cowley, T L McGee, et al.
Experimental Eye Research|May 1, 1985
Glial cell component in retinoblastomaJ L Craft, D N Sang, T P Dryja, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 1, 1985
Accuracy of detection of the retinoblastoma gene by esterase D linkageS L Halloran, J A Boughman, T P Dryja, et al.
Investigative Ophthalmology & Visual Science|April 1, 1994
In vivo transfer of a reporter gene to the retina mediated by an adenoviral vectorT Li, M Adamian, D J Roof, et al.
Genomics|September 1, 1993
Complete genomic sequence of the human retinoblastoma susceptibility geneJ Toguchida, T L McGee, J C Paterson, et al.
Nature|October 16, 1986
A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcomaS H Friend, R Bernards, S Rogelj, et al.
Ophthalmology|September 15, 1999
Intraocular-central nervous system lymphoma: clinical features, diagnosis, and outcomesE K Akpek, I Ahmed, F H Hochberg, et al.
Investigative Ophthalmology & Visual Science|August 1, 1990
Analysis of genes coding for S-antigen, interstitial retinol binding protein, and the alpha-subunit of cone transducin in patients with retinitis pigmentosaP J Ringens, M Fang, T Shinohara, et al.
Pageof 15