Answer:
The chromosomes are arranged in their respective homologous pairs. In humans, this displays 22 pairs of autosomes and 1 pair of sex chromosome.
Explanation:
Chromosomes that are similar in their size and shape and also display similar genetic traits and carry the same genetic information are paired together. These are known as homologous chromosomes. These chromosomes carry different variations of similar genes in them. In humans there are 46 chromosomes in total. These chromosomes are paired and form 23 homologous pairs. Among these 23 homologous pairs, 22 pairs are autosomes and one pair are the sex chromosomes which are either (XX or XY). The sex chromosomes determine the sex of an individual. XX chromosomes represent a female and XY chromosomes represent a male.
Learn more about autosomes here:
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Completed part of the questionErrors in copying can result in changes in the DNA sequence that could be inherited by future generation.
Answer:
DNA stores genetic information in the sequence of its bases
DNA can be replicated by making complementary copies of each strand
Errors in copying can result in changes in the DNA sequence that could be inherited by future generation.
Explanation:
<u>the fact that DNA is located in the Nucleus is not related to double strands.</u>
<u>the DNA csn change is not relevant ,</u>
<u> therefore the above 3 options are the correct answers.</u>
Answer:
that would be a phenotype
Yes because a compound is a chemical bond with two or more different atoms with will create a chemical reaction but with just elements those don’t really chemically react to one another
That is phsycogenic i know from personal experience
