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Genomics
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November 15, 2001
Evolutionary breakpoints on human chromosome 21
M T Davisson, L J Bechtel, E C Akeson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 19, 2000
The bst locus on mouse chromosome 16 is associated with age-related subretinal neovascularization
R S Smith, S W John, A Zabeleta, et al.
Cytogenetics and Cell Genetics
|
August 31, 2001
Ts65Dn -- localization of the translocation breakpoint and trisomic gene content in a mouse model for Down syndrome
E C Akeson, J P Lambert, S Narayanswami, et al.
Investigative Ophthalmology & Visual Science
|
October 23, 1997
Decreased retinal ganglion cell number and misdirected axon growth associated with fissure defects in Bst/+ mutant mice
D S Rice, Q Tang, R W Williams, et al.
Genomics
|
January 8, 1999
Patchy fur, a mouse coat mutation associated with X-Y nondisjunction, maps to the pseudoautosomal boundary region
O Korobova, P W Lane, J Perry, et al.
Vision Research
|
February 21, 2002
Retinal degeneration mutants in the mouse
B Chang, N L Hawes, R E Hurd, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
November 1, 1996
A new mouse mutation causing male sterility and histoincompatibility
P F Ward-Bailey, K R Johnson, M A Handel, et al.
Cytogenetics and Cell Genetics
|
January 1, 1990
Report of the comparative subcommittee for human and mouse homologies
M T Davisson, P A Lalley, J Peters, et al.
Genomics
|
July 1, 1997
Genetic and physical maps of the stargazer locus on mouse chromosome 15
V A Letts, A Valenzuela, J P Kirley, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
December 31, 1997
Birthdate and cell marker analysis of scrambler: a novel mutation affecting cortical development with a reeler-like phenotype
J L González, C J Russo, D Goldowitz, et al.
Page
of 14
Search research articles
Search
Showing results (81-90 of 139) with videos related to
Sort By:
Page
of 14
Genomics
|
November 15, 2001
Evolutionary breakpoints on human chromosome 21
M T Davisson, L J Bechtel, E C Akeson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 19, 2000
The bst locus on mouse chromosome 16 is associated with age-related subretinal neovascularization
R S Smith, S W John, A Zabeleta, et al.
Cytogenetics and Cell Genetics
|
August 31, 2001
Ts65Dn -- localization of the translocation breakpoint and trisomic gene content in a mouse model for Down syndrome
E C Akeson, J P Lambert, S Narayanswami, et al.
Investigative Ophthalmology & Visual Science
|
October 23, 1997
Decreased retinal ganglion cell number and misdirected axon growth associated with fissure defects in Bst/+ mutant mice
D S Rice, Q Tang, R W Williams, et al.
Genomics
|
January 8, 1999
Patchy fur, a mouse coat mutation associated with X-Y nondisjunction, maps to the pseudoautosomal boundary region
O Korobova, P W Lane, J Perry, et al.
Vision Research
|
February 21, 2002
Retinal degeneration mutants in the mouse
B Chang, N L Hawes, R E Hurd, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
November 1, 1996
A new mouse mutation causing male sterility and histoincompatibility
P F Ward-Bailey, K R Johnson, M A Handel, et al.
Cytogenetics and Cell Genetics
|
January 1, 1990
Report of the comparative subcommittee for human and mouse homologies
M T Davisson, P A Lalley, J Peters, et al.
Genomics
|
July 1, 1997
Genetic and physical maps of the stargazer locus on mouse chromosome 15
V A Letts, A Valenzuela, J P Kirley, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
December 31, 1997
Birthdate and cell marker analysis of scrambler: a novel mutation affecting cortical development with a reeler-like phenotype
J L González, C J Russo, D Goldowitz, et al.
Page
of 14