A) Copy the following sentence "The process of meiosis produces (how many?) genetically (identical/different?), (haploid/diploid?) (somatic cells/gametes?) This happened because (1/2) round(s) of division occurred."

b) Answer the five highlighted parts of the sentence by writing in the answers, then remove the words that do not apply so that the sentence makes sense about meiosis.

c) Use the TEXT ENTRY option to post your final sentence.

DO NOT ANSWER THE QUESTION IF YOU DONT UNDERSTAND JUST COMMENT AND ILL EXPLAIN IF YOU DO ILL REPORT.

Meiosis creates 4 unique haploid gametes through 2 rounds of divison.

Explanation:Gametes are created to make genetically different daughter cells.In the first round the homologous chromosomes are split so 2 cells with two chromosomes are created.In the second round the two cells undergo divison again and the chromosomes are split and 4 cells are created with half the DNA.

Hope this helps!

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.

a scenario where a cell may be needed to perform a form of endocytosis is when transporting large molecules. a scenario where a cell may be needed to perform a form of exocytosis is when releasing the large molecule from the cell.