To determine the fractions you are asking about, let's analyze the possible offspring of an Xx female and an XY male:
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Parental Genetic Makeup:
- Female: Xx (one unaffected X and one affected X)
- Male: XY (one X and one Y)
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Offspring Genotypes: When an Xx female and an XY male have children, you can set up a Punnett square to visualize the combinations:
| | X | Y | |--------|----|----| | X | XX | XY | | x | Xx | xY |
The possible genotypes for the children are:
- XX (unaffected female)
- XY (unaffected male)
- Xx (carrier female, unaffected)
- xY (affected male)
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Count of Offspring Combinations: From the Punnett square, we can see:
- 1 XX
- 1 Xy
- 1 Xx
- 1 xY
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Outcomes:
- Fraction of children with an affected chromosome:
In this case, the affected chromosome is "x". Looking at the combinations:
- XX = unaffected (0 affected chromosomes)
- XY = unaffected (0 affected chromosomes)
- Xx = has 1 affected chromosome
- xY = has 1 affected chromosome
So, 2 out of 4 possibilities (Xx and xY) have an affected chromosome.
Therefore, the fraction of offspring with an affected chromosome is \( \frac{2}{4} = \frac{1}{2} \).- Fraction of children likely to be affected by hemophilia:
Affected individuals will show hemophilia if they have the genotype "xY".
Only one possibility out of the four results in hemophilia:
- xY = affected male
Therefore, the fraction of offspring likely to be affected by hemophilia is \( \frac{1}{4} \).
- Fraction of children with an affected chromosome:
In this case, the affected chromosome is "x". Looking at the combinations:
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Conclusion: The final answer is:
- Fraction of offspring with an affected chromosome: \( \frac{1}{2} \)
- Fraction of offspring likely to be affected by hemophilia: \( \frac{1}{4} \)
So, the correct response is:
- 1 half and 1 fourth.