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About one child in 2,500 is born with phenylketonuria ( an inability to metabolize the amino acid phenylalanine). This is known to be a recessive autosomal trait.
a) If the population in Hardy-Weinberg equilibrium for this trait, what is the frequency of the phenylketonuria allele?
b) What proportion of the population are carriers of the phenylketonuria allele (that is, what proportion are heterozygous)?
What will be appearance of the offspring of a cross of the F1 peaches back to that smooth,oval glanded parent. How several diploid Drosophila cells would be needed to have 1 picomole of each allele.
what is the probability that two cousins who are both carries of a deleterious allele will have a homozygous recessive child with the disease? explain thanks.
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