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Investigative Ophthalmology & Visual Science
|
August 1, 1995
Clinical expression correlates with location of rhodopsin mutation in dominant retinitis pigmentosa
M A Sandberg, C Weigel-DiFranco, T P Dryja, et al.
Nature Genetics
|
July 1, 1993
Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness
T P Dryja, E L Berson, V R Rao, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
July 1, 1989
Identification and significance of multinucleate tumor cells in retinoblastoma
M A Howard, T P Dryja, D S Walton, et al.
Investigative Ophthalmology & Visual Science
|
March 1, 1997
Evaluation of the human gene encoding recoverin in patients with retinitis pigmentosa or an allied disease
A H Parminder, A Murakami, G Inana, et al.
Nature
|
August 4, 1983
Somatic inactivation of genes on chromosome 13 is a common event in retinoblastoma
R Godbout, T P Dryja, J Squire, et al.
Nature
|
September 5, 1991
Oncogenic germ-line mutations in Sp1 and ATF sites in the human retinoblastoma gene
T Sakai, N Ohtani, T L McGee, et al.
Documenta Ophthalmologica. Advances in Ophthalmology
|
February 29, 1984
Visual acuity development in tyrosinase negative oculocutaneous albinism
S G Jacobson, I Mohindra, R Held, et al.
American Journal of Human Genetics
|
November 5, 1997
Evidence that the penetrance of mutations at the RP11 locus causing dominant retinitis pigmentosa is influenced by a gene linked to the homologous RP11 allele
T L McGee, M Devoto, J Ott, et al.
Genomics
|
August 1, 1996
Characterization and chromosomal localization of the gene for human rhodopsin kinase
S C Khani, M Abitbol, S Yamamoto, et al.
The American Journal of Surgical Pathology
|
February 15, 2001
Bilateral diffuse uveal melanocytic proliferation associated with extraocular cancers: review of a process particularly associated with gynecologic cancers
F Chahud, R H Young, J F Remulla, et al.
Page
of 15
Search research articles
Search
Showing results (71-80 of 141) with videos related to
Sort By:
Page
of 15
Investigative Ophthalmology & Visual Science
|
August 1, 1995
Clinical expression correlates with location of rhodopsin mutation in dominant retinitis pigmentosa
M A Sandberg, C Weigel-DiFranco, T P Dryja, et al.
Nature Genetics
|
July 1, 1993
Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness
T P Dryja, E L Berson, V R Rao, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
July 1, 1989
Identification and significance of multinucleate tumor cells in retinoblastoma
M A Howard, T P Dryja, D S Walton, et al.
Investigative Ophthalmology & Visual Science
|
March 1, 1997
Evaluation of the human gene encoding recoverin in patients with retinitis pigmentosa or an allied disease
A H Parminder, A Murakami, G Inana, et al.
Nature
|
August 4, 1983
Somatic inactivation of genes on chromosome 13 is a common event in retinoblastoma
R Godbout, T P Dryja, J Squire, et al.
Nature
|
September 5, 1991
Oncogenic germ-line mutations in Sp1 and ATF sites in the human retinoblastoma gene
T Sakai, N Ohtani, T L McGee, et al.
Documenta Ophthalmologica. Advances in Ophthalmology
|
February 29, 1984
Visual acuity development in tyrosinase negative oculocutaneous albinism
S G Jacobson, I Mohindra, R Held, et al.
American Journal of Human Genetics
|
November 5, 1997
Evidence that the penetrance of mutations at the RP11 locus causing dominant retinitis pigmentosa is influenced by a gene linked to the homologous RP11 allele
T L McGee, M Devoto, J Ott, et al.
Genomics
|
August 1, 1996
Characterization and chromosomal localization of the gene for human rhodopsin kinase
S C Khani, M Abitbol, S Yamamoto, et al.
The American Journal of Surgical Pathology
|
February 15, 2001
Bilateral diffuse uveal melanocytic proliferation associated with extraocular cancers: review of a process particularly associated with gynecologic cancers
F Chahud, R H Young, J F Remulla, et al.
Page
of 15