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:
The answer is 300.
Explanation:
When we cross GG and gg, 100% of the offspring will be heterozygous. If the heterozygotes show 75% penetrance meaning that there is a 75% probability that the plant that has the G gene will actually show it in it's phenotype.
So that means that 75% of the offspring should have dark green color, which means that 300 plants will have the expected phenotype and 100 will not.
I hope this answer helps.
Answer:
36 chromosomes in each cell
Explanation:
Mitosis is an equational division which means that it does not reduce or change the number of chromosomes in the daughter cells. Mitosis in a single parent cell produces two daughter cells each having the same DNA content and the number of chromosomes is present in the parent cell. Each chromosome after the S phase has two sister chromatids that separate from each other and are segregated to the opposite poles of the cell during anaphase of mitosis. Therefore, a cell with 36 chromosomes will form two daughter cells after one round of mitosis. Each daughter cell would have 36 chromosomes.
One cell produces two genetically identical daughter cells is both mitosis and meiosis.
Your answer is gravitational forces
