The kingdoms are Archaebacteria, Eubacteria, Protista, Fungi, Plantae, and Animalia.
<span>The nurse should let the patient know that with every pregnancy, there is actually 50 percent chance of a carrier passing on under this condition or being a carrier.
But not all pregnancies may result to this. The sex of the child will have a great impact on the outcome and it cannot be as a result of the previous pregnancy.
Haemophilia is being termed as an inherited genetic disorder. It results from much to people who bleed longer after an injury. There are two types of hemophilia.
For example, hemophilia A which occurs if there is no enough clot factor VIII. The other one is hemophilia B which occurs if there is no enough clot factor IX.</span>
The result of Telophase 1 and Cytokinesis is two haploid daughter cells that are genetically different from the original cell.
Light rays passes through the pupil in the eye and activates the neurons in the retina. The light wavers that are from the reflection of the object are transformed into neural impulses or transduction then action potentials are released when electrical charges are sent through the neurons. Excitatory neurotransmitters are supplied when action potential goes to the axon terminal and the thalamus routes the neural message from the retina elsewhere in the brain. Feature detectors organize the visual projection of the object.
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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