A defect in stomatin is the main cause of hereditary spherocytosis.
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Q8: Spherocytes may enter the circulation via a
Q9: Bite cells are formed from:
A)The spleen "pitting"
Q10: Spherocytes do not function well in the
Q11: Individuals with Fanconi's anemia characteristically will have:
A)Intravascular
Q12: Red blood cells that are rigid, provide
Q14: Spherocytes differ from normal cells in all
Q15: The RBC inclusions that are composed of
Q16: An eccentric "puddling" of a red blood
Q17: Cholelithiasis is a frequent complication of patients
Q18: An osmotic fragility test is performed on
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