Abstract
| - The retinal dystrophy gene, rdy, in the rat displays autosomal linkage of 19.0 ± 1.7 percent with nonagouti, a, and 31.8 ± 4.1 percent with Svp-1 in linkage group IV. The data are consistent with the linear order rdy—a—Svp-1, but the orientation of this sequence with respect to the centromere is not known. A congenic strain has been developed from some of the testcross animals in which retinal dystrophic and heterozygous control rats of both pink-eyed and black-eyed phenotypes can be distinguished with pigmentation marker genes.
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