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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

✍ Scribed by K. Indrak; J. Indrakova; F. Kutlar; D. Pospisilova; I. Sulovska; E. Baysal; T. H. J. Huisman


Publisher
Springer
Year
1991
Tongue
English
Weight
671 KB
Volume
63
Category
Article
ISSN
0939-5555

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