Posttranscriptional defects in beta-globin messenger RNA metabolism in beta-thalassemia: abnormal accumulation of beta-messenger RNA precursor sequences. [PDF]
, 1981 E J Benz +4 more
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Effect of booklet and combined method on parents' awareness of children with β-thalassemia major disorder [PDF]
, 2008 OBJECTIVE: To assess the effects of booklet and combining methods (lecture, video, etc.) on parents' awareness of children with beta-thalassemia major disorder.
Hasanpour-Dehkordi, A. +1 more
core
Beta Thalassemia and Translation of Globin Messenger RNA
, 1971 David G. Nathan +3 more
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Hemoglobin Mississippi (beta 44ser----cys). Studies of the thalassemic phenotype in a mixed heterozygote with beta +-thalassemia. [PDF]
, 1987 Martin H. Steinberg +6 more
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Renal tubular dysfunction with nephrocalcinosis in a patient with beta thalassemia minor
Saudi Journal of Kidney Diseases and Transplantation, 2008 Thalassemia is a hereditary anemia resulting from defect in hemoglobin production. Beta thalassemia is due to impaired production of beta globin chains, leading to a relative excess of alpha globin chains.
Prabahar Murugesan +4 more
doaj
Beta O-39 thalassemia gene: a premature termination codon causes beta- mRNA deficiency without affecting cytoplasmic beta-mRNA stability [PDF]
, 1984 R. Keith Humphries +4 more
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International Journal of Laboratory Hematology, Volume 47, Issue 3, Page 373-375, June 2025.
Sara Sacchetti +4 more
wiley +1 more source
Relative stability of alpha- and beta-globin messenger RNAs in homozygous beta+ thalassemia.
, 1977 AW Nienhuis, Paul Turner, EJ Jr Benz
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A family with segregating triplicated alpha globin loci and beta thalassemia [PDF]
, 1983 R Galanello +5 more
openalex +1 more source
Delineation of the molecular basis of delta- and normal HbA2 beta- thalassemia [PDF]
, 1988 Paolo Moi +7 more
openalex +1 more source