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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It splits down the middle
<span>viruses reproduce by attaching to a host cell and injecting their nucleic acid into the host cells chromosome, then they can either stay dormant or the will take over the cell, reproduce and then burst out of the cell which kills the host cell </span>
A. cold water with high salt content. The colder the water the more dense it is (ice is pretty dense). Adding salt to a liquid also makes it more dense.
Answer:
Nucleic Acid Amplification Test
Explanation:
A Nucleic Acid Amplification Test or NAATs is a test that is performed to check the smaller amount of DNA that may be in viruses and bacteria.
After this check the sequenced DNA can be compared to known sequences of these specific organisms to discover if they are new organisms or just a variation of an existing one.