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_____ is due to autoimmune production of IgG against GPIIb/IIIa
Burkitt lymphoma classically presents as an extranodal mass in a _____ or young adult (age group)
Hereditary _____ is diagnosed by the osmotic fragility test
T-ALL is characterized by lymphoblasts (TdT+) that express markers ranging from CD-_____ to CD-8
Ig_____-mediated immune hemolytic anemia usually causes extravascular hemolysis
In _____ deficiency, oxidative stress precipitates denaturated hemoglobin as Heinz bodies
The _____ Coombs test adds donor blood and anti-Ig antibody (Coombs reagent) to the patient's serum
When exposed to conditions that favor the _____ form of Hemoglobin, HbS polymerizes and forms needle-like structures ("sickle cells")
Diffuse Large B-Cell Lymphoma is most commonly caused by alterations in _____ or Bcl-6
_____ measures the intrinsic and common pathways of the coagulation cascade
Anemias: Classification and Approach
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Hemolytic Anemias
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Myeloproliferative Neoplasms
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Myelodysplastic Syndromes
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Acute Leukemias
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Chronic Leukemias
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Lymphomas and Lymphoid Neoplasms
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Plasma Cell Disorders
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Bleeding Disorders
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Thrombotic Disorders
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