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F W Fitzke

Showing results (131-140 of 135) with videos related to

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The British Journal of Ophthalmology|November 1, 1994
Ocular findings associated with a 3 base pair deletion in the peripherin-RDS gene in autosomal dominant retinitis pigmentosaJ J Wroblewski, J A Wells, A Eckstein, et al.
Human Gene Therapy|October 30, 1999
High-titer recombinant adeno-associated virus production from replicating amplicons and herpes vectors deleted for glycoprotein HX Zhang, M De Alwis, S L Hart, et al.
Cell Death & Disease|March 3, 2011
Imaging multiple phases of neurodegeneration: a novel approach to assessing cell death in vivoM F Cordeiro, L Guo, K M Coxon, et al.
The British Journal of Ophthalmology|March 20, 2004
An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 geneS S Dandekar, N D Ebenezer, C Grayson, et al.
Ophthalmology|January 27, 2000
Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclaseK Gregory-Evans, R E Kelsell, C Y Gregory-Evans, et al.
Pageof 14

Showing results (131-140 of 135) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 135 results.
The British Journal of Ophthalmology|November 1, 1994
Ocular findings associated with a 3 base pair deletion in the peripherin-RDS gene in autosomal dominant retinitis pigmentosaJ J Wroblewski, J A Wells, A Eckstein, et al.
Human Gene Therapy|October 30, 1999
High-titer recombinant adeno-associated virus production from replicating amplicons and herpes vectors deleted for glycoprotein HX Zhang, M De Alwis, S L Hart, et al.
Cell Death & Disease|March 3, 2011
Imaging multiple phases of neurodegeneration: a novel approach to assessing cell death in vivoM F Cordeiro, L Guo, K M Coxon, et al.
The British Journal of Ophthalmology|March 20, 2004
An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 geneS S Dandekar, N D Ebenezer, C Grayson, et al.
Ophthalmology|January 27, 2000
Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclaseK Gregory-Evans, R E Kelsell, C Y Gregory-Evans, et al.
Pageof 14