Betty Ciesla

General Description of the Hemoglo-binopathies

Sickle Cell Anemia

Genetics and Incidence of Sickle Cell Anemia Pathophysiology of the Sickling Process Clinical Considerations for Sickle Cell Anemia Disease Management and Prognosis Laboratory Diagnosis Sickle Cell Trait

Hemoglobin C Disease and Trait and Hemoglobin SC

Variant Hemoglobins of Note

Hemoglobin S-beta thalassemia Hemoglobin E

Hemoglobin DPunjab/Hemoglobin G phila

Hemoglobin OArab

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