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If a haemophilic man marries a carrier w...

If a haemophilic man marries a carrier woman than which of the following holds true for their progenies ?

A

50 % daughters are carrier and 50 % are haemophilic

B

All the daughters are haemophilic

C

All sons are haemophilic and all daughters are normal

D

All sons normal, all daughters carriers

Text Solution

AI Generated Solution

The correct Answer is:
To solve the problem of determining the genetic outcomes for the progeny of a hemophilic man and a carrier woman, we can follow these steps: ### Step 1: Understand the Genetic Background - Hemophilia is an X-linked recessive disorder. This means that the gene responsible for hemophilia is located on the X chromosome. - Males have one X and one Y chromosome (XY), while females have two X chromosomes (XX). ### Step 2: Identify the Genotypes - The hemophilic man has the genotype X^hY, where X^h represents the X chromosome carrying the hemophilia gene. - The carrier woman has the genotype X^hX, where one X chromosome carries the hemophilia gene (X^h) and the other is normal (X). ### Step 3: Determine Gametes - The man can produce two types of gametes: X^h (from his X chromosome) and Y (from his Y chromosome). - The woman can produce two types of gametes: X^h (from her hemophilic X) and X (from her normal X). ### Step 4: Create a Punnett Square - Set up a Punnett square to visualize the possible combinations of gametes from the parents. | | X^h (from mother) | X (from mother) | |---------|--------------------|------------------| | X^h (from father) | X^hX^h (daughter, hemophilic) | X^hX (daughter, carrier) | | Y (from father) | X^hY (son, hemophilic) | XY (son, normal) | ### Step 5: Analyze the Results - From the Punnett square, we can see the possible genotypes of the offspring: - 1 daughter with genotype X^hX^h (hemophilic) - 1 daughter with genotype X^hX (carrier) - 1 son with genotype X^hY (hemophilic) - 1 son with genotype XY (normal) ### Step 6: Calculate the Ratios - The results show: - 50% of the daughters are carriers (X^hX) - 50% of the daughters are hemophilic (X^hX^h) - 50% of the sons are hemophilic (X^hY) - 50% of the sons are normal (XY) ### Conclusion The correct statement regarding their progeny is that 50% of the daughters are carriers and 50% are hemophilic.

To solve the problem of determining the genetic outcomes for the progeny of a hemophilic man and a carrier woman, we can follow these steps: ### Step 1: Understand the Genetic Background - Hemophilia is an X-linked recessive disorder. This means that the gene responsible for hemophilia is located on the X chromosome. - Males have one X and one Y chromosome (XY), while females have two X chromosomes (XX). ### Step 2: Identify the Genotypes - The hemophilic man has the genotype X^hY, where X^h represents the X chromosome carrying the hemophilia gene. ...
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Knowledge Check

  • A coloured man (X^(c)Y) marries a woman who is carrier for haemophilia (XX^(h)) . Which of the following is true for their progenies ?

    A
    `25 %` female progenies carry the genes foe both haemophilia and colourblindness
    B
    `25 %` male progenies carry only the gene for haemophilia
    C
    `25 %` female progenies carry only the gene for colourblindness
    D
    all of these
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