They will have different traits
Atrioventricular septum is the surface indentation that separates the atria from the ventricles.
<h3>What is an atrioventricular septum? </h3>
The interatrial and interventricular septal cross the atrioventricular annular plane and merge with the septum tricuspid and anterior mitral leaflet attachment at the septal atrioventricular junction, which is a critical region of the heart.
The tricuspid and mitral valves seem cruciate on a four-chamber view when both septa are converging, earning the term crux of the heart, cardiac crux, or crux cordis.
The atrioventricular septum, a septal component dividing the atria from the left ventricle, is a distinctive anatomic characteristic of the atrioventricular junction.
Therefore, the atrioventricular septum is the indentation that separates the atria from the ventricles.
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Answer:
TRUE
Explanation:
When cells divide, they make new cells. A single cell divides to make two cells and these two cells then divide to make four cells, and so on. We call this process "cell division" and "cell reproduction," because new cells are formed when old cells divide
Answer:
Answer is embolism.
Explanation:
Embolism can simply be explained as a critical or serious medical condition which occurs is an obstruction s when there is an obstruction of a blood vessel such as the artery. This means that, the artery becomes blocked because of a foreign substance , usually blod clot which travels through the blood stream.
Note that, when a blood clot travels through the blood stream to the brain, it can result to embolic stroke.
Some of the things that can lodge in the blood vessel to cause blockage are fats from the marrow, air bubbles and collagen.
In chromatin, substitution mutations are most common in linker regions. Option d is the correct answer.
Mutation by substitution When one nucleotide base is replaced by another, this occurs. Mismatch mutation A type of substitution mutation in which a single nucleotide is replaced, resulting in the coding of an incorrect amino acid, which usually results in a malfunctioning protein. Silent mutations are the result of genetic code redundancy (degeneracy): This is false, as silent mutations are the result of a base substitution that has no discernible effect on a protein's amino acid sequence.
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