Please use this identifier to cite or link to this item: 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 M.
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

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