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Proceedings of the National Academy of Sciences of the United States of America
|
September 30, 1998
Effect of vitamin A supplementation on rhodopsin mutants threonine-17 --> methionine and proline-347 --> serine in transgenic mice and in cell cultures
T Li, M A Sandberg, B S Pawlyk, et al.
American Journal of Human Genetics
|
April 29, 1998
Frequency of somatic and germ-line mosaicism in retinoblastoma: implications for genetic counseling
K C Sippel, R E Fraioli, G D Smith, et al.
Human Genetics
|
January 1, 1983
Low incidence of deletion of the esterase D locus in retinoblastoma patients
T P Dryja, G A Bruns, B Gallie, et al.
Genomics
|
July 1, 1991
The human retinal degeneration slow (RDS) gene: chromosome assignment and structure of the mRNA
G H Travis, L Christerson, P E Danielson, et al.
American Journal of Human Genetics
|
April 3, 2001
Null RPGRIP1 alleles in patients with Leber congenital amaurosis
T P Dryja, S M Adams, J L Grimsby, et al.
Cornea
|
June 27, 2003
Histopathology of explanted collar button keratoprostheses: a clinicopathologic correlation
E J Dudenhoefer, M Nouri, I K Gipson, et al.
Investigative Ophthalmology & Visual Science
|
August 31, 2001
Clinical features and mutations in patients with dominant retinitis pigmentosa-1 (RP1)
E L Berson, J L Grimsby, S M Adams, et al.
The New England Journal of Medicine
|
November 8, 1990
Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa
T P Dryja, T L McGee, L B Hahn, et al.
Science (New York, N.Y.)
|
February 17, 1989
Point mutational inactivation of the retinoblastoma antioncogene
J M Horowitz, D W Yandell, S H Park, et al.
Nature
|
January 25, 1990
A point mutation of the rhodopsin gene in one form of retinitis pigmentosa
T P Dryja, T L McGee, E Reichel, et al.
Page
of 15
Search research articles
Search
Showing results (121-130 of 141) with videos related to
Sort By:
Page
of 15
Proceedings of the National Academy of Sciences of the United States of America
|
September 30, 1998
Effect of vitamin A supplementation on rhodopsin mutants threonine-17 --> methionine and proline-347 --> serine in transgenic mice and in cell cultures
T Li, M A Sandberg, B S Pawlyk, et al.
American Journal of Human Genetics
|
April 29, 1998
Frequency of somatic and germ-line mosaicism in retinoblastoma: implications for genetic counseling
K C Sippel, R E Fraioli, G D Smith, et al.
Human Genetics
|
January 1, 1983
Low incidence of deletion of the esterase D locus in retinoblastoma patients
T P Dryja, G A Bruns, B Gallie, et al.
Genomics
|
July 1, 1991
The human retinal degeneration slow (RDS) gene: chromosome assignment and structure of the mRNA
G H Travis, L Christerson, P E Danielson, et al.
American Journal of Human Genetics
|
April 3, 2001
Null RPGRIP1 alleles in patients with Leber congenital amaurosis
T P Dryja, S M Adams, J L Grimsby, et al.
Cornea
|
June 27, 2003
Histopathology of explanted collar button keratoprostheses: a clinicopathologic correlation
E J Dudenhoefer, M Nouri, I K Gipson, et al.
Investigative Ophthalmology & Visual Science
|
August 31, 2001
Clinical features and mutations in patients with dominant retinitis pigmentosa-1 (RP1)
E L Berson, J L Grimsby, S M Adams, et al.
The New England Journal of Medicine
|
November 8, 1990
Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa
T P Dryja, T L McGee, L B Hahn, et al.
Science (New York, N.Y.)
|
February 17, 1989
Point mutational inactivation of the retinoblastoma antioncogene
J M Horowitz, D W Yandell, S H Park, et al.
Nature
|
January 25, 1990
A point mutation of the rhodopsin gene in one form of retinitis pigmentosa
T P Dryja, T L McGee, E Reichel, et al.
Page
of 15