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Compound heterozygosity for a β°-thalassemia (frameshift codons 38/39 ; -C) and a nondeletional Swiss type of HPFH (A→C at NT -110, Gγ) in a Czechoslovakian family
by
INDRAK, K
,
INDRAKOVA, J
,
KUTLAR, F
,
POSPISILOVA, D
,
SULUVSKA, I
,
BAYSAL, E
,
HUISMAN, T. H. J
Published in
Annals of hematology
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Annals Of Hematology
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Anemias. Hemoglobinopathies
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Biological And Medical Sciences
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Diseases Of Red Blood Cells
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Gγ Synthesis
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Hematologic And Hematopoietic Diseases
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Hpfh
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Increased Hb F
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Medical Sciences
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Promoter Mutation
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