Answer: A I think
Explanation: I'am really sorry if i'am wrong
Answer:
Any combination of D, E and F
Explanation:
Since A, B, and C belong to different orders, and D, E and F belong to the same order, the latter are more closely related and thus are expected to show a greater degree of structural homology. They are closer to their common ancestor than A, B and C.
The endosymbiotic theory states that some of the organelles in eukaryotic cells were once prokaryotic microbes. Mitochondria and chloroplasts are the same size as prokaryotic cells and divide by binary fission.
This statement is true.
In the case of autosomal dominant disease, the person is either homozygous (which is very rare) or heterozygous. On the molecular level, either the mutation produced a new deleterious protein for the organism, or the mutation affected an existing protein in the physiological state and that a 50% activity is not enough to compensate for the needs. of the body.
In case of autosomal recessive disease, the sick person is always homozygous. If the two loci each have a different mutant allele, it is called a "composite heterozygote". People with autosomal recessive inheritance disorder have "mandatory heterozygote" parents.