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Sickle cell syndromes: II. The sickle cell anemia-α-thalassemia syndrome

✍ Scribed by George R. Honig; Mabel Koshy; R. George Mason; Loyda N. Vida


Book ID
119456600
Publisher
Elsevier Science
Year
1978
Tongue
English
Weight
839 KB
Volume
92
Category
Article
ISSN
1097-6833

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Sickle cell anemia, sickle cell β-thalas
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We have analyzed the hemoglobin abnormalities in nearly 50 Albanian patients with a significant hemoglobinopathy and included 37 relatives in this study. Sickle cell anemia (SS) is a common disorder; all 15 sickle cell anemia patients had the complications expected for this disease. The beta S haplo