$A$ woman is a carrier for hemophilia (having one gene on each $X$ chromosome) and also carries one gene for color blindness on one $X$ chromosome. She marries a normal man. What will be the phenotype of their offspring?

  • A
    All sons and daughters are hemophilic and color-blind.
  • B
    Color-blind and hemophilic daughters.
  • C
    $50\%$ hemophilic,color-blind sons and $50\%$ hemophilic sons.
  • D
    $50\%$ hemophilic daughters and $50\%$ color-blind daughters.

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Similar Questions

If a color-blind man marries a normal woman,then regarding the vision of their offspring,which of the following is true?

Select the correct options for the given statements:
Statements:
$X$: Formation of Haemoglobin is controlled by two closely linked genes $HBA1$ and $HBA2$ on chromosome $16$ of each parent.
$Y$: $\beta$-Thalassemia is controlled by a single gene $HBB$ on chromosome $21$ of each parent.

Given below are two statements:
Statement $I$: The son of a carrier woman has a $100$ percent chance of being colour blind.
Statement $II$: $A$ daughter of a carrier mother and a normal father will be $100$ percent colour blind.
In the light of the above statements,choose the correct answer from the options given below:

The following pedigree chart shows:

Which of the following conditions is harmful in itself but also provides protection against a mosquito-borne infectious disease?

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