The mouse mutation ulnaless on chromosome 2.
Chromosome-Mapping, Crosses-Genetic, Extremities, Female, Heterozygote, Linkage-(Genetics), Male, Mice, Mice-Inbred-Strains, Mutation, Phenotype, Reproduction, Support-Non-U, S, -Gov't, Support-U, S, -Gov't-Non-P, H, S, Support-U, S, -Gov't-P, H, S
J Hered 1990 Mar-Apr;81(2):151-3.
The dominant skeletal mutation ulnaless (Ul) in the mouse causes extreme reduction of the radius and ulna and deformities of the tibia and fibula. Penetrance appears to be complete, but the homozygote is not known, as heterozygous males do not breed. We report the linkage of the Ul gene on Chromosome 2, 18 cM proximal to pallid (pa), and describe its phenotypic effects.
Davisson, M T. and Cattanach, B M., " The mouse mutation ulnaless on chromosome 2." (1990). Faculty Research 1990 - 1999. 58.
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