Alpha thalassemia is a hemoglobinopathy on account of decreased manufacturing of the α-globin protein from loss of as much as 4 α-globin genes, with one or two lacking in the trait phenotype. Individuals with sickle cell illness who co-inherit the loss of one or two α-globin genes have been recognized…
Ca+ncer stem cell markers
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calcium chloride transformation
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calcium chloride competent cells
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calcium resorption
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Ca+lcein am protocol
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cacl2 transformation
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Ca+rdiomyocyte markers
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bzip transcription factor
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Ca+ncer pathways
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