Computer simulation showing the effects of relaxed selection and assortative mating on the Cx gene, beginning in 1800 with a generation time of 20 years. A, Frequency of Cx homozygotes in the presence (solid line) and absence (dotted line) of assortative mating; B, Frequency of a common recessive deafness gene (Cx) and two rare genes, either linked at 1 cM (Gene A) or unlinked (Gene B) to the Cx locus. A fixed population size of 200,000 and an equal sex ratio were assumed. In B, a mutation-selection balance initially was assumed with frequencies for Cx, A, and B of .01304, .002881, and .002881, respectively. In A and B, the reproductive fitness of the deaf rose from 0 to 1.0 in five generations, whereas assortative mating rose from 0 (random mating) to .9 and remained constant thereafter. To incorporate linguistic homogamy, deaf subjects choosing hearing partners were assumed to select “native signers” who were the offspring of deaf parents, with a probability of .3 by the fifth generation. Such spouses frequently carry multiple nonallelic recessive genes for deafness.