A statement which best supports the choice made in Part A (independent assortment) is: C. The diagram shows four unique gametes that are the result of two chromosomes separating in different ways.
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Mendel's law of independent assortment.</h3>
Mendel's law of independent assortment is a theory which states that the alleles of two or more different genes are sorted into unique gametes that are independent of each another.
This ultimately implies that, the allele that is typically being received by a gamete for one gene doesn't influence or affect the type of allele that is received for another gene.
Based on the biological process (independent assortment) shown in the image attached below for part A, we can infer and logically deduce that a statement which best supports the choice made is that he diagram shows four unique gametes that are the result of two chromosomes separating in different ways.
Read more on independent assortment here: brainly.com/question/2376592
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Your graph is attached.
P.S.: You haven't learned anything about making or using graphs.
Answer:
Golgi apparatus is like the fuel pump on a car. … The vacuole stores waste like the gas tank stores it’s fuel. The ribosome produces protein for the cell as the alternator produces energy for the battery to stay charged.
Explanation:
Hope this helps you out (:
The answer to the question mentioned above is "Synaptic Cleft".
The region composed of a presynaptic cell, its target cell and the space between them is a Synaptic Cell. This cell exists between the neurons and this is a microscopic gap.
Answer:
mother
Explanation:
Hemophilia is a sex-linked recessive disorder caused by a mutation in one of the genes responsible for encoding the clotting factor proteins (factor VIII or factor IX), which are located on the X chromosome. Moreover, the Klinefelter syndrome is caused by men having an additional X chromosome. In this case, the nondisjunction occurred from the mother because her gamete included an extra X, it is for that reason that all genes localized on the X chromosome, including the defective gene involved in hemophilia, can cause all of her sons to be affected by the disease in some generation. Thus, sister chromatids did not separate during meiosis (Anaphase II) and caused two copies of the defective allele for the hemophilia trait.
