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…
parafin embedded
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paraformaldehyde fixation
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paraffin sections protocol
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oligodendrocytes
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SEC23IP
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ST6GALNAC2
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osteocalcin
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okt3 antibody
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pd 1 antibody
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