answer:
During prophase, the complex of DNA and proteins contained in the nucleus, known as chromatin, condenses. The chromatin coils and becomes increasingly compact, resulting in the formation of visible chromosomes. ... The replicated chromosomes have an X shape and are called sister chromatids
Explanation:
The extra X chromosome is received from mother.
<h3><u>Explanation</u>:</h3>
Klinefelter's syndrome is the condition of chromosomal aberration where the person has an extra X chromosome. This means the genotype of the person is 44+XXY and the total chromosome number is 47. This condition is achieved due to inappropriate meiotic division and one of the sperm or ovum has the an extra X chromosome.
Here both the parents are normal in terms of colour vision. So the father cannot have the gene of colour blindness because if it was present, then father would have been colour blind because he has only one X chromosome per cell. So its present in mother who is heterozygous in terms of colour blind gene. So the extra X chromosome also came from her which made the presence of two defective X chromosomes in the offspring and made it colour blind.
Answer: 1). A and B are both dominant (because A and B are codominant to one another)
2). E. All of the above
Explanation:
1). From the image above, A and B are both dominant because they are equally expressed when they occur in a pair (when they occur as blood type AB), also they are dominant because each of them expressed itself when it occurs in a pair with a recessive allele (IAi and IBi).
2). The children of a father with A blood and a mother with B blood will have all the four blood types: A, B, AB, and O. If each parent has a recessive allele, that is if each parent is heterozygous for his/her blood type (IAi for the father and IBi for the mother), the cross between them will produce all the four possible blood types.
See the attached punnet square for more information.
