It is bigger than. Hope this helps
Answer:
IDK SORRY I hAVE DISLEXIA
Explanation:
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.
The most powerful approach to isolating a single mutant from a population of billions is positive selection.
fertilization comes first
it is followed by cleavage which is the rapid cellular division which forms the blastula
then comes gastrulation where the 3 germ layers are formed.
followed by organogenesis which consists first forms the organs and then comes the specialization
Therefore your answer would be B
