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M T Davisson

Showing results (81-90 of 139) with videos related to

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Genomics|November 15, 2001
Evolutionary breakpoints on human chromosome 21M 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 neovascularizationR 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 syndromeE 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 miceD 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 regionO Korobova, P W Lane, J Perry, et al.
Vision Research|February 21, 2002
Retinal degeneration mutants in the mouseB 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 histoincompatibilityP 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 homologiesM T Davisson, P A Lalley, J Peters, et al.
Genomics|July 1, 1997
Genetic and physical maps of the stargazer locus on mouse chromosome 15V 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 phenotypeJ L González, C J Russo, D Goldowitz, et al.
Pageof 14

Showing results (81-90 of 139) with videos related to

Sort By:
Pageof 14
Genomics|November 15, 2001
Evolutionary breakpoints on human chromosome 21M 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 neovascularizationR 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 syndromeE 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 miceD 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 regionO Korobova, P W Lane, J Perry, et al.
Vision Research|February 21, 2002
Retinal degeneration mutants in the mouseB 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 histoincompatibilityP 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 homologiesM T Davisson, P A Lalley, J Peters, et al.
Genomics|July 1, 1997
Genetic and physical maps of the stargazer locus on mouse chromosome 15V 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 phenotypeJ L González, C J Russo, D Goldowitz, et al.
Pageof 14