Answer:
This disorder is caused by a recessive allele, its inheritance is sex-linked.
Explanation:
The disorder affects boys born to unaffected parents, this means that at least one of them has to be a carrier of the allele which causes the disease. So, if the allele was dominant, it would express in parents and sons. But, in this case, only is expressed in sons, so it can´t be dominant. Moreover, this condition has a sex-linked inheritance because it is always seen in boys and never in girls. This happens due to boys only have an X chromosome, so if they inherit the recessive allele of the disease, they will express it. On the other hand, girls have two X chromosomes, so if they inherit one copy of the recessive allele, they will be carriers and they won't be affected.
This disorder is never seen in females because they need to have two copies of the recessive allele. However, to have double copy, they should inherit one copy from their mothers and one copy of their fathers, but boys with the allele are affected and they die in early teens without having progeny. Therefore, a girl can't have a "carrier-father", so they will never have two copies to express the disorder.
A. Cytoplasm
(The Nucleus is the control, site of DNA)
Cell wall is in plant cells, giving stability and protecting the cell from rupturing. DNA is stored in the Nucleus, not a organelle.
The answer is Cytoplasm, C.
id say the first one and the third one, sorry if it’s wrong
Answer:
69.7%
Explanation:
Adenine base pairs with thymine
guanine base pairs with cytosine
you need to get to 100%
30.3-100=69.7%
There will be 30.3% or adenine and thymine and 69.7% or guanine and cytosine.
