The gene for colour blindness is located on

  • A
    Homologous part of $X$-chromosome
  • B
    Non-homologous part of $X$-chromosome
  • C
    Homologous part of $Y$-chromosome
  • D
    Non-homologous part of $Y$-chromosome

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Similar Questions

What is the probability of having a color-blind male child from two normal parents?

Which of the following cannot be included in Mendelian disorders?

Hemophilia is more common in human males than in females because it is a:

Identify the genetic disorders based on the following characteristics:
$(i)$ Presence of sickle-shaped $RBC$.
$(ii)$ Blood does not clot,leading to non-stop bleeding.
$(iii)$ The heterozygous female transmits the disease to sons.
$(iv)$ Both heterozygous parents transmit the disease to offspring.

If a colour blind lady marries a normal man,their children will be:

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