Organisms with 23 different chromosome pairs can produce gametes with 8 million possible chromosome combinations, an incredible amount of genetic variation. This
many chromosome combinations in the gametes is possible because of which of the
following?
O thousands of different types of DNA base pairs.
O random separation of chromosomes during meiosis.
O mutations that lead to more chromosomes in the gametes.
O crossing-over that occurs during mitosis.

i'm gonna put a couple so you can chose from

explanation:

if you know the fur color of the offspring mice, you can use the ratios to identify the genotypes of the parents.

if either parent mouse passes a dominant allele, the offspring will have black fur.

if the parental mice has two different fur color (i.e white and black) , the color of the offspring's fur would be either black, white, or the combination of both (grey)

hope this : )

golgi body just took the test on edge

an individual’s sex (i.e., whether they are a male or female) is determined by the sex chromosomes. most people have two sex chromosomes, one that is inherited from their mother and one that is inherited from their father. typically, females have two x chromosomes (xx) and males have one x chromosome and one y chromosome (xy). conditions caused by changes (“mutations”) in genes located on the x chromosome are considered x-linked.

x-linked recessive inheritance

most x-linked conditions are recessive. this means that in a person with two x chromosomes (most females), both copies of a gene (i.e., one on each x chromosome) must have a change or mutation whereas in a person with one x chromosome (most males), only one copy of a gene must have a mutation. a female with a mutation in one copy of a gene on the x chromosome is said to be a “carrier” for an x-linked condition. a male with a mutation in a gene on the x chromosome is typically affected with the condition. because females have two copies of the x chromosome and males have only one x chromosome, x-linked recessive diseases are more common among males than females. however, x-linked recessive diseases can occur in both males and females.

for x-linked recessive disorders, an unaffected carrier mother who has a mutation in a gene on the x chromosome can transmit either the x chromosome with this mutation or a “normal” x chromosome to her children. if the father is unaffected, none of her daughters will be affected and all of her daughters will be unaffected—since they will inherit at least one normal x chromosome from their father. however, each daughter will have a 50% chance of being an unaffected carrier like her mother and a 50% chance of both x chromosomes being normal.