“…In beta thalassemia the young cells contain less hemoglobin F (2,3) and, if the patient is splenectomized, more insoluble membrane-bound inclusions of precipitated alpha chains (4)(5)(6)(7). In hemoglobin H disease, the young cells contain more soluble hemoglobin H, whereas inclusions of precipitated beta chains are detected in the older cells (1,4,8,9).…”