Answer:
mutation in DNA
Explanation:
Mutations are changes in the genetic code that can occur in many ways. Each time a cell divides, say, DNA must be copied into two copies, one copy for each new cell. Although this copying is very precise, it is still not perfect - for about every billion accurately copied databases, one is mistranslated.
Another source is DNA damage, which can occur spontaneously through the normal life of the cell, or through external toxins or negative influences (ultraviolet radiation, for example). Through evolution, cells have developed a very complex system for repairing changes in DNA, but these systems not only have limitations but can sometimes cause additional errors themselves.
The fetus can be screened for abnormalities using karyotyping and biochemical analysis using amniocentesis and chorionic villus sample.
<h3>What data can we glean from CVS and amniocentesis?</h3>
In at-risk fetuses, these tests can detect genetic illnesses such cystic fibrosis, Tay-Sachs disease, and sickle cell disease. The main benefit of CVS over amniocentesis is that it is done considerably earlier in pregnancy—at 10 to 13 weeks as opposed to 15 to 20 weeks—thus saving more time for the mother.
<h3>What can a couple learn about their growing fetus from amniocentesis and chorionic villus sampling?</h3>
Amniocentesis and chorionic villus sampling (CVS) are prenatal diagnostic techniques used to identify certain fetal genetic disorders. The likelihood of miscarriage rises with both procedures.
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Answer:
B. There will be two cells each with 36 chromosomes.
Explanation:
The products of mitosis are called diploid cells, and they each have the complete set of chromosomes. These cells are usually important for activities such as growth, repair etc. They make up our normal body (somatic) cells. Therefore, the answer is 36, only 36 matches the description of genetically identical cells
Answer:
T~T
Explanation:
sowwy I can't, I can't see them very well but just guess and google the ones you can, good luck!!