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https://www.um.edu.mt/library/oar/handle/123456789/82555
Title: | Developmental hematology of SS and SC disease in association with α-thalassemia-2 |
Authors: | Felice, Alex Marino, E. M. McKie, Kathleen Mood McKie, Virgil C. |
Keywords: | Hemoglobin Hemoglobinopathy Thalassemia Molecular microbiology |
Issue Date: | 1985 |
Publisher: | American Society of Hematology |
Citation: | Felice, A., Marino, E. M., McKie, K. M., & McKie, V. C. (1985). Developmental hematology of SS and SC disease in association with α-thalassemia-2. Blood, 56 (1), Supplement 1, 59a. |
Abstract: | The nuber and organization of the α, ζ and γ globin genes have been determined on the DNA of 400 patients attending the Pediatric Sickle Cell Clinics of our Center. The patients were participating in long-term prospective studies on possible effects of α-thal on the hecatological changes accompanying postnatal development. CBC and Hb composition were obtained in the steady state on patients of different ages and correlated with the number of α globin genes. |
URI: | https://www.um.edu.mt/library/oar/handle/123456789/82555 |
Appears in Collections: | Scholarly Works - FacM&SSur |
Files in This Item:
File | Description | Size | Format | |
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Developmental_hematology_of_SS_and_SC_disease_in_association_with_α-thalassemia-2_1985.pdf | 1.75 MB | Adobe PDF | View/Open |
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