The answer to this question is B
1.) Achodroplasia is a autosomal dominant disorder, the suspected case suggested that inorder for the parents to produce and offspring with achondroplasia. One parents must have a single mutant gene of achodroplasia to be inherited by his offspring. for this case, It is suggested that the offspring might have developed its own mutant gene as it only affect 1 in 25,000 birth. There is changes of genes during early development.
2.) The mother said that they don't have that history of disorder. again, it's autosomal dominant disorder. one parents must have that kind of disorder so their child can also inherit it. Thus, no of the childs parents is a carrier.
Answer:
Part A....B
Part B....C
Explanation:
It should be understood that Mice are always first used to clinical test especially for drugs or other things that are supposed to be for human use, this is because Mice and human genetic disorders have arisen from conserved and related evolutionary processes. Therefore, when the clinical trial or test produces a positive result in the Mice, it is almost certain that the result will be the same in human.
Now in part B. When the result result is different, it might be because of the differences in anatomy and physiology might hide or change development and symptoms of disease. And that is the reason why, the result of a particular drug differs from person to person.
They can’t live in dry areas because fungi need to be able to trap moisture since their broad tops can dry out
