Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/82314
Title: α-Thalassemia among pediatric Nb S homozygotes
Authors: Felice, Alex
Zhao, J.
Kutlar, A.
McKie, Kathleen M.
McKie, Virgil C.
Keywords: Hemoglobin
Hemoglobinopathy
Sickle cell anemia
Molecular microbiology
Issue Date: 1987
Publisher: American Society of Hematology
Citation: Felice, A., Zhao, J., Kutlar, A., McKie, K. M., & McKie, V. C. (1987). α-Thalassemia among pediatric Nb S homozygotes. Twenty-ninth Annual Meeting of the American Society of Hematology, Washington, DC. 61a
Abstract: The number of α globin genes have been documented among 255 active SS patients under the age of 15 years. Ascertainment in the area served by our clinical program is 84%. The common -3.7 Kb α+ -Thalassemia (Th) had a gene frequency of 0.17. The incidence of homozygotes was 2.9%, and heterozyqotes 30.6%. These values are consistent with Hardy-Weinberg expectations.
URI: https://www.um.edu.mt/library/oar/handle/123456789/82314
Appears in Collections:Scholarly Works - FacM&SSur

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