Molecular characterization of β-thalassemia in Czechoslovakia
- 1 February 1992
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 88 (4) , 399-404
- https://doi.org/10.1007/bf00215673
Abstract
No abstract availableKeywords
This publication has 38 references indexed in Scilit:
- 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 familyAnnals of Hematology, 1991
- Treatment of advanced chronic lymphocytic leukemia by fludarabineAnnals of Hematology, 1991
- HB Köln or α2β298(FG5)VAL→MET in a Czechoslovakian FamilyHemoglobin, 1991
- HB E [β26(B8)GLU→LYS] in a Czechoslovakian FamilyHemoglobin, 1991
- FREQUENCIES OF COMMON β-THALASSAEMIA ALLELES AMONG DIFFERENT POPULATIONS: VARIABILITY IN CLINICAL SEVERITYBritish Journal of Haematology, 1990
- β-Thalassemia RepositoryHemoglobin, 1990
- Frameshift Codon 5 [FSC-5 (−CT)] Thalassemia; a Novel Mutation Detected in a Greek PatientHemoglobin, 1989
- Hb Oloc or α2β286(F2)Ala → Asp, A New High Oxygen Affinity VariantHemoglobin, 1987
- Hb Saint Louis or α2β228(B10)Leu→Gln in a Czechoslovakian MaleHemoglobin, 1986
- Further Nodification of the Mtcrochromatographic Deternination of Hemoglobin AHemoglobin, 1977