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: Node
Explanation:
Cladograms are a graphical representation of the evolutionary relationship between organisms. These are usually shown as branches from a central point, which represents a common ancestor. In rooted cladograms, the branches are shown relative to the time elapsed since evolving from a common ancestor joined at the node, or point of divergence.
Evolution typically occurs after accumulating mutation, and natural selection of beneficial traits that confer greater chances for survival.
Answer:
the wood is being burnt leaving behind ash and changing a solid to a gas ( wood to fire )
Explanation:
Increased frequency of homozygous genotypes
