The answer you chose is correct becAuse if both parents are heterozygous for a disease that is recessive there is a 25%chance of the offspring inheriting the trait.Ex:
R r
R (RR) (Rr)
r (Rr) (rr) rr is the only outcome that can inherit the disease.
Answer:
A
Explanation:
I think it is A because of there being cell walls
Answer:
B. Nearly every amino acid translated after the error will create the wrong protein after the deletion of a base.
Explanation:
Generally, mutations occur in two ways: 1) a base replacement, where one base is replaced for another; 2) insertion or deletion, where a base is either incorrectly inserted or deleted from a codon.
When a nucleotide is wrongly inserted or deleted from a codon, the effects of this change can be extreme. An insertion or deletion can affect every codon in a particular genetic sequence. For example, given the code:
GAU GAC UCC GCU AGG. It is the codes for the amino acids aspartate, aspartate, serine, alanine, and arginine. If the A in the GAU were to be deleted, the code would become GUG ACU CCG UAG G. It won't produce any right amino acid.
So, if the code becomes changes, it won't produce any amino acid or will produce the wrong amnio acid.
Answer:
1. vi. Preganglionic
2. vii. adrenergic
3. ii. sympathetic chain ganglia
4. iii. Craniosacral
5. viii. splanchnic
Explanation:
Action potential travel down preganglionic nerve fibre. They travel towards Vagus Nerve near the effector organ. These impulses arrive at cardiac plexus, which create action potential in postganlianic.
