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You are examining the following human pedigree and want to determine if the rare dominant disease allele (D) is linked to a specific DNA sequence location, referred to as a "molecular marker." You are using two molecular markers, R1 and R2.Parental and progeny genotypes and phenotypes are indicated.Note that the father is a dihybrid at both loci, but the mother is homozygous recessive at both loci and linked to R1 (d-R1/d-R1) .There is complete penetrance of the trait and a linkage phase of D-R1/d-R2 in the father.Assuming that the marker and the gene are linked, what is the best estimate of the map distance between the two loci?
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