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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I’m not sure but it might be the third one
Yes the answer would be true
The answer is Glycolysis. Glycolysis is the first stage of Respiration that happens in the cytoplasm of the cell. In this process, a 6-carbon sugar molecules is broken down to form 2 molecules of 3-carbon pyruvate. The process of Glycolysis generates ATP in the presence of oxygen.
Substances that are made up of only one type of atom.
