Answer:Nucleoid
⬜Nucleus
⬜Mitochondria
⬜Chloroplast
Circular DNA (in nucleoid)
⬜DNA in nucleus
⬜Endoplasmic Reticulum
⬜Golgi Apparatus Flagella Cila
Explanation
That's weird, they all are...
The presentation of an 18-month-old with hereditary fructose intolerance (HFI), deficiency of aldolase B and low blood glucose levels is due to accumulation of fructose-1 phosphate and the inhibition of glycolytic-gluconeogenic pathways.
Explanation:
Hereditary fructose intolerance leads to deficiency of fructose-1-phosphate aldolase enzyme. This enzyme deficiency leads to accumulation of fructose-1 phosphate in the liver. Fructose-1 phosphate inhibits the action of phosphorylase enzyme which monitors the glycogen to glucose conversion. Since glucose formation is reduced, hypoglycemia and lactic acidosis takes place accounting for the patient’s low blood sugar.
1. what clue to the presence of certain genetic disorders can be seen in karyotype? 2. why might a lab worker attempting to diagnose a genetic disorder prefer to work with photographs of chromosomes rather than the chromosome themselves? 3.why would it be much difficult to construct a karyotype of unstained chromosomes?
That refers to the planet Neptune.
Hope it helps!
