Colorblindness in humans is a mutation carried on the X chromosome. A man and woman with normal vision have a colorblind son. What are the chances their next child will be a colorblind daughter?
Colorblindness in humans is a mutation carried on the X chromosome. A man and woman with normal vision have a colorblind son. What are the chances their next child will be a colorblind daughter?
what are the options that have to match them to?
The answer is either 3 or 4
They’re chances would be 20
The chances are very high
Explanation:
Because Color blindness is carried on the X chromosome and females usually have 2 X chromosomes the female Is more likely to have colorblindness than the males.