B-monomer
I am not sure about the second one but i think it's C
1.b
2.d
3.a
this is the answer to your qeustion.
Answer:
I would say it is B.
Explanation:
In Meiosis, specifically in Prophase 1, it creates genetic variation. Crossing over occurs in that stage
There is going to be a 25% chance of it being heterozygous unless both parents are heterozygous then if so you do happen to have to heterozygous parents it will be 100% heterozygous.
The color blindness would be from his mother, since it is located in the X chromosome, and since his father is not color blind, and he only has one X chromosome, it could not come from him, but since the trait is recessive in women (meaning that it is covered up by a capital X) it means his mother could have the trait in one of her chromosomes, but not the other. Unfortunately Bob got the short end of the stick and got the chromosome with color blindness, and since men only have one X chromosome, it is dominant in men, leaving Bob with color blindness.
