You are examining a family in which both parents are known to be carriers for s…

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You are examining a family in which both parents are known to be carriers for sickle cell anemia, which is a rare autosomal recessive disease with 2% of the population carrying the mutant allele. Their first child was born with the disease, and the parents have come to you to assess whether the new fetus is also diseased, is a carrier, or is homozygous normal. DNA samples from each family member and the fetus are tested by PCR and gel electrophoresis. The following results are obtained:
  1. What is the probability that the child who will develop from this fetus will exhibit the disease?
  2. When this child grows up and mates, what is the probability that any one of her children will be afflicted with the disease?
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