The Answer Is 27% . . . . . . . . . . . . . The dots are so I can post the answer, because without a long reply I can't answer.
Answer:
No, the child cannot inherit the disease.
Explanation:
The problem tells you that the man has a recessive allele for an inherited disease, but he has a normal phenotype. This means that the disease is recessive and in order for an individual to have the disease, they must have two recessive copies of the allele. The problem also tells you that the mother has a genotype that does not include this allele. With this information, you can do a punnet cross of BB (mother) x Bb (carrier father), and end up with the following possible genotypes: BB, Bb, BB, Bb. Therefore the child will not have the disease, but there is a 50% chance that the child will be a carrier for the disease.
Changes in a DNA sequence that affect genetic information are known as mutations.
Answer:
Receiving sensory information and carrying commands to the muscles.
Explanation:
The spinal cord serves as the transmission conduit for the passage of action potential as sensory information through the sensory/afferent neurons to the dorsal roots of the spinal cord.The information synapse with the inter neurons,branching off to the brain and emerged as the response through the motor/efferent neurons to the effectors(muscles).
This pathways is called reflex arc. Thus most of the involuntary action of the body is conducted through the spinal cord