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In humans, a very rare dominant allele that causes the linle finger to be crooked has a penetrance of 80%. In other words, 80% of heterozygotes carrying the allele will have a crooked linle finger. If a homozygous unaffected person has children with a heterozygote carrying this mutant allele, what is the probability that
1. One offspring will have a linle finger that is crooked?
2. At least one of three offspring will have a crooked linle finger?
3. At least one of four offspring will have a normal linle finger?
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