| hemoglobin E–thalassemia d. |
a hereditary condition involving simultaneous heterozygosity for hemoglobin E and thalassemia, manifested by mild hemolytic anemia and persistent splenomegaly; called also hemoglobin E–thalassemia.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hemoglobin H d. |
α-thalassemia in individuals heterozygous for hemoglobin H, characterized by chronic hemolytic anemia associated with splenomegaly; red blood cell hypochromia, anisocytosis, and poililocytosis are accompanied by inclusion bodies detectable by supravital staining.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hemoglobin S–t. |
sickle cell–thalassemia disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hemoglobin SC d. |
sickle cell–hemoglobin C d.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hemoglobin SD d. |
sickle cell–hemoglobin D d.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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