The alpha thalassemias result from:
A) Gene deletion
B) Defective alpha genes
C) Iron overload
D) Excessive production of alpha chains
Correct Answer:
Verified
Q2: All of the following are symptoms of
Q5: Transferrin receptors for iron uptake are located
Q8: The first stage of iron deficiency anemia
Q8: Ringed sideroblasts in the bone marrow are
Q9: The alpha thalassemic condition that is incompatible
Q11: Storage iron is usually determined by the:
A)
Q12: What is the presumptive clinical condition?
A) Pernicious
Q12: Failure to thrive, facial structure abnormalities, severe
Q14: A 15-year-old Lebanese boy was sent
Q17: The presence of which hemoglobin will result
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