6 results on '"Masala, B"'
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2. The C→G transition in the α2-globin gene of a normal αα-chromosome is responsible for the Hb G-Philadelphia variant in Sardinians
3. DiminishedAγTfetal globin levels in Sardinian haplotype II β°-thalassaemia patients are associated with a four base pair deletion in theAγTpromoter
4. Haemoglobin phenotypes of the wild European mouflon sheep living on the island of Sardinia
5. Sardinian Haplotype II β0‐Thalassemia Is Linked to the Variant AγT‐Globin Gene with a 4‐Bp Promoter Deletion and Diminished AγT Expressiona,b,
6. The level of Hb F-sardinia (α2A γ275IIe→Thr) in the fetal hemoglobin of sardinian β-thalassemic homozygotes determined by isoelectric focusing
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