In a marriage between a female "carrier" of red-green color blindness and a normal male, what proportion of their male progeny will have the trait?

Explore the Mendelian Link Test. Study with questions and explanations, comprehend Mendel's principles, genetic inheritance, and related concepts. Prepare confidently for your exam!

In considering a marriage between a female carrier of red-green color blindness and a normal male, we start by understanding the genetics behind this trait. Red-green color blindness is an X-linked recessive trait, which means the gene responsible for the condition is located on the X chromosome.

The female carrier has one normal X chromosome and one affected X chromosome, which can be designated as X^N (normal) and X^c (color blind). The normal male has one X chromosome (X^N) and one Y chromosome (Y).

When a carrier female and a normal male have offspring, their daughters will inherit one X chromosome from each parent, while their sons will inherit their X chromosome from the mother and a Y chromosome from the father. The possible combinations for their male progeny are:

  • From the mother: X^N or X^c

  • From the father: Y

This results in two potential genotypes for their male offspring:

  1. X^N Y (normal vision)

  2. X^c Y (color blind)

Since the carrier mother can pass either X chromosome equally, there is a 50% chance that a son will inherit the affected chromosome (X^c), and a 50% chance he will

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