Answer:
the female sea otter has 1
Explanation:
Answer:
One-half of the daughters of an affected man would have this condition.
Explanation:
Each daughter born to a woman that is positive for a dystrophin mutation on one of her two X chromosomes possess a 50 percent likelihood of possessing the mutation and also becoming a carrier. Carriers at times do not show the disease symptoms but may give birth to a child that has the mutation or the disease condition. DMD carriers do have a higher chance of cardiomyopathy.
A man with DMD cannot transfer the affected gene to his sons since he passes to his son a Y chromosome, not the X chromosome. But he will definately transfer it to his daughters, since each daughter possess her father’s only X chromosome resulting in the daughters being carriers.
Hence, One-half of the daughters of an affected father and a carrier mother could have this condition.
Answer:
<em>They will have a large number of genetic variations.</em>
Explanation:
Genetic variations arise due to sexual reproduction or due to the process of meiosis.
Cross-pollination can be described as a process in which the pollen of one flower is transferred to another flower. The pollen when fertilizes the egg in the stigma, will produce offspring with varied genetic characteristics. This will be because the pollen would carry the trait of another flower and the egg of another flower. This will lead to many genetic variations.