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irga5000 [103]
3 years ago
7

In familial hypercholesterolemia, individuals homozygous for the allele causing the disorder completely lack receptors on liver

cells that take up cholesterol from the blood stream. Heterozygotes have one-half the number of receptors while individuals homozygous for the normal allele are phenotypically normal. This is the example of what?A. Complete dominance.B. Co-dominance.C. Incomplete dominance.D. Epistasis.
Biology
1 answer:
Finger [1]3 years ago
8 0

Answer:

the correct option is the C

Explanation:

This happens when two paired alleles do not match because one could not express on the paired allele. What happens is that there will be a third phenotype that will occur.

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The human genome comprises about 3 x 109 base pairs of DNA, and no two humans, other than identical twins, ever have been or wil
arsen [322]

Answer:

The correct answer is C.

Explanation:

The amount of genetic variation in two humans is 0.1 percent of their genome. Human genetic variation refers to the biological difference that exists in the human population.

The genetic variation in humans and apes genome is about 4 percent which is 35 million differences in a single nucleotide.

The genetic variation between apes and humans (Homo sapiens), according to scientists includes gene expression differences, variation in the transportable elements and type and number of repetitive genomic DNA transportable elements, the difference in the gene sequence, single nucleotide polymorphic, etc.

According to research, 97 percent of humans and orangutans genomes are identical. Based on evolution, among all apes, the orangutans are very special as it has been stable for the past 15 million years.

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