To know what happens here, you need to analyze the alleles.
If the father is color blind and the daughter is not, you can suppose that is a recessive allele.
You can tell she is a carrier only, and because we received one sexual allele from each parent. If they ask you about the gender, we can suppose a cross between Xx and XY being lower x the recessive allele (color-blind vision).
When you draw the Punnett square, you'll found the probabilities are XX, XY, Xx, and xY.
So, you have a 50% chance of having a boy and 25% chance of having a color-blind boy.
Answer:
option B
Explanation:
there are 22 pair of autosome and 2 pair of sex chromosome
The statement " Each gene in the human genome codes for a single protein. "is just wrong, as according to the basic knowledge of human genome, o<span>nly about 2 percent of the genome codes for proteins. This answer does make difference and clearly explaines why the previous one is wrong. Hope you will find it helpful!</span>
Answer:
Phenylketonuria, Cystic Fibrosis and Sickle Cell Anemia, these all are disorders caused by hereditary mutation.
Hope it helps!
Gaurd cells are high for exchange of gad
