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International Ophthalmology Clinics
|
January 1, 1982
Lacrimal gland tumors: a clinicopathological analysis of 160 cases
C Ni, S C Cheng, T P Dryja, et al.
Nature Genetics
|
December 2, 1999
Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa
H Morimura, F Saindelle-Ribeaudeau, E L Berson, et al.
Investigative Ophthalmology & Visual Science
|
October 23, 1997
Dominant and digenic mutations in the peripherin/RDS and ROM1 genes in retinitis pigmentosa
T P Dryja, L B Hahn, K Kajiwara, et al.
Experimental Eye Research
|
August 1, 1997
Evaluation of the rhodopsin kinase gene in patients with retinitis pigmentosa
S Yamamoto, S C Khani, E L Berson, et al.
American Journal of Human Genetics
|
August 12, 1999
No mutations in the coding region of the PRKCG gene in three families with retinitis pigmentosa linked to the RP11 locus on chromosome 19q
T P Dryja, J McEvoy, T L McGee, et al.
Human Genetics
|
January 1, 1984
Chromosome 13 restriction fragment length polymorphisms
T P Dryja, J M Rapaport, R Weichselbaum, et al.
Investigative Ophthalmology & Visual Science
|
September 1, 2000
Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa
T P Dryja, J A McEvoy, T L McGee, et al.
Nucleic Acids Research
|
January 11, 1990
Detection of the XbaI RFLP within the retinoblastoma locus by PCR
T L McGee, G S Cowley, D W Yandell, et al.
American Journal of Ophthalmology
|
November 1, 1978
Melanocytic tumor of the anterior uvea
E B Dunphy, T P Dryja, D M Albert, et al.
Experimental Eye Research
|
November 1, 1991
Genetic analysis of patients with retinitis pigmentosa using a cloned cDNA probe for the human gamma subunit of cyclic GMP phosphodiesterase
P R Cotran, G A Bruns, E L Berson, et al.
Page
of 15
Search research articles
Search
Showing results (51-60 of 141) with videos related to
Sort By:
Page
of 15
International Ophthalmology Clinics
|
January 1, 1982
Lacrimal gland tumors: a clinicopathological analysis of 160 cases
C Ni, S C Cheng, T P Dryja, et al.
Nature Genetics
|
December 2, 1999
Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa
H Morimura, F Saindelle-Ribeaudeau, E L Berson, et al.
Investigative Ophthalmology & Visual Science
|
October 23, 1997
Dominant and digenic mutations in the peripherin/RDS and ROM1 genes in retinitis pigmentosa
T P Dryja, L B Hahn, K Kajiwara, et al.
Experimental Eye Research
|
August 1, 1997
Evaluation of the rhodopsin kinase gene in patients with retinitis pigmentosa
S Yamamoto, S C Khani, E L Berson, et al.
American Journal of Human Genetics
|
August 12, 1999
No mutations in the coding region of the PRKCG gene in three families with retinitis pigmentosa linked to the RP11 locus on chromosome 19q
T P Dryja, J McEvoy, T L McGee, et al.
Human Genetics
|
January 1, 1984
Chromosome 13 restriction fragment length polymorphisms
T P Dryja, J M Rapaport, R Weichselbaum, et al.
Investigative Ophthalmology & Visual Science
|
September 1, 2000
Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa
T P Dryja, J A McEvoy, T L McGee, et al.
Nucleic Acids Research
|
January 11, 1990
Detection of the XbaI RFLP within the retinoblastoma locus by PCR
T L McGee, G S Cowley, D W Yandell, et al.
American Journal of Ophthalmology
|
November 1, 1978
Melanocytic tumor of the anterior uvea
E B Dunphy, T P Dryja, D M Albert, et al.
Experimental Eye Research
|
November 1, 1991
Genetic analysis of patients with retinitis pigmentosa using a cloned cDNA probe for the human gamma subunit of cyclic GMP phosphodiesterase
P R Cotran, G A Bruns, E L Berson, et al.
Page
of 15