The probability that their son exhibits the 'color blind' trait is 0%. It is a type of inheritance linked to the X chromosome.
<h3>Inheritance linked to the X chromosome</h3>
In men, the patterns of inheritance linked to the X chromosome don't follow conventional mendelian inheritance because men have only one X chromosome.
Conversely, women have two X chromosomes, thereby the inheritance pattern resembles Mendelian inheritance.
It is important to highlight that color blindness is a recessive trait on the X chromosome.
In this case, the mother is a carrier, thereby the probability of passing this trait as a carrier to her son is 50%, whereas the father is normal, thereby the probability of passing this trait to his son is 0%.
Learn more about inheritance linked to the X chromosome here:
brainly.com/question/1020249
Answer:
Both heterozygous, with the trait for short hair being dom over the long hair
Explanation:
25% would be homzygous dominant, 25% homzygous recessive and 50% heterozygous
i think this is wrong but i tried
B. Increased exposure to UV light increases the risk of mutation occurring.
These circular DNA molecules are called C: Plasmids
Since the client is diagnosed of having right sided brain attack or also known as stoke, since the client is right handed, the most difficult task that the client would perform is having to do activities that involves of using his right side of the body such as his or her right arm, hands or right leg.
