హేమోగ్లోబిన్ యొక్క తప్పు సంశ్లేషణ కారణంగా రక్తహీనత యొక్క వారసత్వ రూపం,

Noun:

తలన్రేలు చేయు,

thalassaemia's Usage Examples:

"Hb E/beta-thalassaemia: a common " clinically diverse disorder".

provide some genetic resistance to malaria including sickle cell disease, thalassaemias, glucose-6-phosphate dehydrogenase, and possibly others.

thalassaemia who are not frequently transfused.

"Safety and effectiveness of thalidomide and hydroxyurea combination in β‐thalassaemia intermedia and major: a retrospective pilot study".

theoretically help to reduce the need for blood transfusions in people with thalassaemia major or intermedia but there is currently no reliable evidence from clinical.

Homozygote α0 thalassaemias, where numerous γ4 but no α-globins occur at all (referred to as Hb.

was known for his hematological and clinical studies of Hemoglobin E/β-thalassaemia and was an elected fellow of the National Academy of Medical Sciences.

theoretically help to reduce the need for blood transfusions in people with thalassaemia major or intermedia but there is currently no reliable evidence from.

Alpha-thalassemia (α-thalassemia, α-thalassaemia) is a form of thalassemia involving the genes HBA1 and HBA2.

hemoglobinopathies like sickle cell disease, sickle cell C disease, and sickle cell thalassaemia disease.

can occur in sickling hemoglobinopathies like sickle cell disease, sickle cell C disease, and sickle cell thalassaemia disease.

, The Westminster contribution to the correction of thalassaemia major and other inborn anaemias.

Consequences included natural selection for sickle-cell disease, thalassaemias, glucose-6-phosphate dehydrogenase deficiency, Southeast Asian ovalocytosis.