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Genomics|August 15, 1996
Chromosomal localization of a new mouse lens opacity gene (lop18)B Chang, N L Hawes, R S Smith, et al.Biochemical Genetics|December 1, 1982
Pleiotropic and other genetic effects influencing the activities of brain and liver enzymes in congenic lines of C57BL/6J mice with defined electrophoretic variant markersR J Feuers, J B Bishop, L J McGarrity, et al.Experimental Biology and Medicine (Maywood, N.J.)|September 25, 2001
Maximum life spans in mice are extended by wild strain allelesS Klebanov, C M Astle, T H Roderick, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|August 1, 1987
Mapping X-linked ophthalmic diseases. III. Provisional assignment of the locus for blue cone monochromacy to Xq28R A Lewis, J D Holcomb, W C Bromley, et al.Biochemical Genetics|August 1, 1976
Evolution of mammalian carbonic anhydrase loci by tanden duplication: close linkage of Car-1 and Car-2 to the centromere region of chromosome 3 of the mouseE M Eicher, R H Stern, J E Womack, et al.Genetica|January 5, 2002
Heritability of life span in mice and its implication for direct and indirect selection for longevityS Klebanov, K Flurkey, T H Roderick, et al.Proceedings of the National Academy of Sciences of the United States of America|November 21, 1995
Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15J R Heckenlively, B Chang, L C Erway, et al.Molecular Vision|September 24, 1999
Identification of a missense mutation in the alphaA-crystallin gene of the lop18 mouseB Chang, N L Hawes, T H Roderick, et al.Investigative Ophthalmology & Visual Science|March 1, 1994
Retinal degeneration in motor neuron degeneration: a mouse model of ceroid lipofuscinosisB Chang, R T Bronson, N L Hawes, et al.Investigative Ophthalmology & Visual Science|February 1, 1996
Corn1: a mouse model for corneal surface disease and neovascularizationR S Smith, N L Hawes, S D Kuhlmann, et al.Pageof 6