Shown in Figure 19-22 is a genetic pedigree of a family with several members affected by a heritable disease.Affected individuals are shown in black and healthy individuals are shown in white.Males are shown as boxes and females as circles.Can a single mutation explain the pattern of inheritance? Is the mutation responsible for the disease dominant or recessive? Is the mutation carried on the X chromosome, the Y chromosome, or an autosome?
Figure 19-22
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