sickle cell-hemoglobin C disease

sickle cell-hemoglobin C disease

References in periodicals archive ?
Red cell life span in sickle cell-hemoglobin C disease with a note about sickle cell-hemoglobin 0 ARAB.
Acute splenic complications in children with sickle cell-hemoglobin C disease.
The most common types include hemoglobin SS (homozygous) disease, sickle cell-hemoglobin C disease, and the sickle beta-thalassemia syndromes[1].