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dc.contributor.authorFelice, Alex-
dc.contributor.authorMarino, E. M.-
dc.contributor.authorMcKie, Kathleen M.-
dc.contributor.authorMcKie, Virgil C.-
dc.date.accessioned2021-10-21T09:26:05Z-
dc.date.available2021-10-21T09:26:05Z-
dc.date.issued1985-
dc.identifier.citationFelice, 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.en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar/handle/123456789/82555-
dc.description.abstractThe 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.en_GB
dc.language.isoenen_GB
dc.publisherAmerican Society of Hematologyen_GB
dc.rightsinfo:eu-repo/semantics/openAccessen_GB
dc.subjectHemoglobinen_GB
dc.subjectHemoglobinopathyen_GB
dc.subjectThalassemiaen_GB
dc.subjectMolecular microbiologyen_GB
dc.titleDevelopmental hematology of SS and SC disease in association with α-thalassemia-2en_GB
dc.typeconferenceObjecten_GB
dc.rights.holderThe copyright of this work belongs to the author(s)/publisher. The rights of this work are as defined by the appropriate Copyright Legislation or as modified by any successive legislation. Users may access this work and can make use of the information contained in accordance with the Copyright Legislation provided that the author must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the prior permission of the copyright holder.en_GB
dc.description.reviewedpeer-revieweden_GB
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