Biochemical Characterisation of Spectrum of Hemoglobinopathies and Thalassemia Syndromes - Experience with 689 Cases in a Tertiary Care Hospital in South India


The inherited diseases of hemoglobin have remarkable phenotypic variability because of genetic modifiers necessitating medical intervention at various stages of disease. Genotype–phenotype relationship is crucial in this regard. So three year retrospective study of biochemical pattern of Hemoglobinopathies and Thalassemias and their clinical manifestations… (More)


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