The four phases in the life cycle of a cell and place the events in order, starting with events that occur immediately after the cell was born are:
- The first gap (G1)
- The synthesis (S)
- The second gap (G2)
- M
<h3>What is a cell?</h3>
A cell can be defined as simplest, basic, functional and structural unit of life
In conclusion, the four phases in the life cycle of a cell and place the events in order, starting with events that occur immediately after the cell was born are:
first gap (G1), synthesis (S) scond gap (G2) and M
Learn more about cells:
brainly.com/question/2622341
#SPJ1
A gene is <u>Co</u><u>d</u><u>e for a trait, </u><u>are</u><u> </u><u>small</u><u> </u><u>sections</u><u> </u><u>with</u><u> </u><u>DNA</u><u> </u><u>strand</u><u>,</u><u> </u><u>Are</u><u> </u><u>blueprints</u><u> </u><u>for</u><u> </u><u>proteins</u><u>.</u>
- <em>Therefore</em><em>,</em><em> </em><em>Option</em><em> </em><em>D</em><em>.</em><em> </em><em>All</em><em> </em><em>of</em><em> </em><em>the</em><em> </em><em>above</em><em> </em><em>is</em><em> </em><em>correct</em><em>!</em><em>!</em><em>~</em>
Answer:
If a female child has hemophilia it is possible that the mother is a carrier of the hemophilia gene and the father has hemophilia.
Explanation:
- A daughter gets X chromosome from both her parents.
- It is generally seen in males.
- Hemophilia is generally recessive in females.They act as carriers of hemophilia. This occurs because they have a X chromosome that dominates the hemophilia affected gene that they inherit from any parent.
- But, if both the parents have faulty genes ,i.e the mother is the carrier of the gene and the father is hemophiliac, then the chances are the daughter has hemophilia too.