Answer:
Restoring force is a force which acts to bring a body to its equilibrium position. The restoring force is a function only of position of the mass or particle, and it is always directed back toward the equilibrium position. Therefore the restoring force of air particles should be displaced in the direction of the force and according to Newton 3rd law of motion, once the force is removed, restoring force of elasticity returns the displaced particle to a resting state .
That its not in the cell or that its just there or that you can't find it anywhere else but in the body outside the cell....
A.The genotype frequencies can be determined by dividing the number of individuals with a genotype by the total number all the individuals.
FF genotype frequency:
98÷200=0,49. There are approximately 5 <span>homozygous dominant mice in 10.
Ff genotype frequency:
84</span>÷200=0,42. There are approximately 4 <span>heterozygous mice in 10.
ff genotype frequency:
18</span>÷200=0,09. There are approximately 1 <span>homozygous recessive mouse in 10.
B.To determine the frequency of an allele we can divide the number of times that the allele appears by the total number of alleles.
F allele frequency:
</span>

<span>=0.7
There are 7 F alleles in 10 random alleles.
f </span>allele frequency:

=0.3
There are 3 f alleles in 10 random alleles.<span>
</span>
Answer:
b. Frank received the mutant chromosome from his father. Nondisjunction occurred in his father during the first meiotic division.
Explanation:
As you can see in the question above, Frank has Klinefelter syndrome which causes him to have normal skin patches and skin patches without sweat glands. Her mother has completely normal hair, which may indicate that the defective gene was not supplied by her. In addition, Frank's father has anhydrotic ectodermal dysplasia, an X-linked condition where the skin does not contain sweat glands.
Although Frank's father's defective gene is linked to the X chromosome, it is likely that Frank inherited the defective gene from his country. This may have occurred because during meiosis I, his father's genes did not show disjunction. As a result, Frank presents a mosaic of his phenotype, because an inactivation of the X chromosome occurred.