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American Journal of Medical Genetics
|
January 1, 1986
Mouse chromosome fragility
M M Sanz, E C Jenkins, W T Brown, et al.
Investigative Ophthalmology & Visual Science
|
May 14, 1998
Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice
S W John, R S Smith, O V Savinova, et al.
Cytogenetics and Cell Genetics
|
July 28, 2001
Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene
S A Cook, E C Akeson, C Calvano, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 15, 1991
FVB/N: an inbred mouse strain preferable for transgenic analyses
M Taketo, A C Schroeder, L E Mobraaten, et al.
Nature Genetics
|
April 7, 1999
Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice
B Chang, R S Smith, N L Hawes, et al.
Investigative Ophthalmology & Visual Science
|
September 1, 2000
Retinal degeneration 6 (rd6): a new mouse model for human retinitis punctata albescens
N L Hawes, B Chang, G S Hageman, et al.
Cytogenetics and Cell Genetics
|
January 1, 1987
Report on the committee on comparative mapping
P A Lalley, S J O'Brien, N Créau-Goldberg, et al.
Cytogenetics and Cell Genetics
|
January 1, 1989
Report of the committee on comparative mapping
P A Lalley, M T Davison, J A Graves, et al.
Nature Genetics
|
April 1, 1996
Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation
M Burmeister, J Novak, M Y Liang, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 11, 2000
A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse
N B Akhmedov, N I Piriev, B Chang, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 82) with videos related to
Sort By:
Page
of 9
American Journal of Medical Genetics
|
January 1, 1986
Mouse chromosome fragility
M M Sanz, E C Jenkins, W T Brown, et al.
Investigative Ophthalmology & Visual Science
|
May 14, 1998
Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice
S W John, R S Smith, O V Savinova, et al.
Cytogenetics and Cell Genetics
|
July 28, 2001
Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene
S A Cook, E C Akeson, C Calvano, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 15, 1991
FVB/N: an inbred mouse strain preferable for transgenic analyses
M Taketo, A C Schroeder, L E Mobraaten, et al.
Nature Genetics
|
April 7, 1999
Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice
B Chang, R S Smith, N L Hawes, et al.
Investigative Ophthalmology & Visual Science
|
September 1, 2000
Retinal degeneration 6 (rd6): a new mouse model for human retinitis punctata albescens
N L Hawes, B Chang, G S Hageman, et al.
Cytogenetics and Cell Genetics
|
January 1, 1987
Report on the committee on comparative mapping
P A Lalley, S J O'Brien, N Créau-Goldberg, et al.
Cytogenetics and Cell Genetics
|
January 1, 1989
Report of the committee on comparative mapping
P A Lalley, M T Davison, J A Graves, et al.
Nature Genetics
|
April 1, 1996
Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation
M Burmeister, J Novak, M Y Liang, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 11, 2000
A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse
N B Akhmedov, N I Piriev, B Chang, et al.
Page
of 9