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Chromosoma|December 29, 1975
Chromosome markers in Mus musculus: differences in C-banding between the subspecies M.m. musculus and M.m. molossinusV G Dev, D A Miller, R Tantravahi, et al.
The Journal of Experimental Zoology|August 1, 1992
Genetic linkage analysis of the murine developmental mutant velvet coat (Ve) and the distal chromosome 15 developmental genes Hox-3.1, Rar-g, Wnt-1, and Krt-2C P Hart, J G Compton, S H Langley, et al.
Genetics|February 1, 1988
The Hox-2 homeo box gene complex on mouse chromosome 11 is closely linked to ReC P Hart, D K Dalton, L Nichols, et al.
Visual Neuroscience|December 8, 2005
Mouse models of ocular diseasesB Chang, N L Hawes, R E Hurd, et al.
Genomics|March 8, 2000
Lop12, a mutation in mouse Crygd causing lens opacity similar to human Coppock cataractR S Smith, N L Hawes, B Chang, et al.
American Journal of Medical Genetics|January 1, 1986
Mouse chromosome fragilityM 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 miceS 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 geneS 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 analysesM 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 miceB Chang, R S Smith, N L Hawes, et al.
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