Answer:
The correct answer is - incomplete dominance.
Explanation:
A inheritance pattern that is characterized by pattern in which the one allele is not completely dominant over the its recessive variant of the allele and due to its incomplete dominance a third phenotype expressed over, termed as the incomplete dominance.
In the case of the familial hypercholesterlemia, it is genetic disorder in which the individual lacks the receptors on liver cells remove cholesterol from the blood. This condition occur in the homozygous allele case. In normal people have receptors normal while in heterozygous condition individual have half of the total receptors.
Thus, it is the case of incomplete dominance.
Answer:
Autosomal dominant pattern.
Explanation:
If the pattern of inheritance is same in the disease just like the model of colorblindness mutation so we can say that the disease has autosomal dominant pattern because the colorblindness mutation also occur due to the autosomal dominant pattern. Sometimes the disease is also inherited from their parents through genetically. So both diseases and the model colorblindness mutation are considered same if both have the same pattern of inheritance.
Answer:
2. The liquid iron and nickel outer core's motion in relation to the metallic solid inner core becomes a geodynamo.
Explanation:
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The answer to the question is:
C-<span>The more complex a living thing the more chromosomes it is likely to have
Hope this helps!! :-)</span>