HB Monroe or α2β230(B12)ARG→THR, a Variant Associated with β-Thalassemia due to a G→C Substitution Adjacent to the Donor Splice Site of the First Intron
- 1 January 1989
- journal article
- research article
- Published by Taylor & Francis in Hemoglobin
- Vol. 13 (1) , 67-74
- https://doi.org/10.3109/03630268908998053
Abstract
(1989). HB Monroe or α2β230(B12)ARG→THR, a Variant Associated with β-Thalassemia due to a G→C Substitution Adjacent to the Donor Splice Site of the First Intron. Hemoglobin: Vol. 13, No. 1, pp. 67-74.This publication has 22 references indexed in Scilit:
- Analysis of enzymatically amplified β-globin and HLA-DQα DNA with allele-specific oligonucleotide probesNature, 1986
- Separation of normal and abnormal hemoglobin chains by reversed-phase high-performance liquid chromatographyJournal of Chromatography A, 1986
- Haplotypes and levels of fetal hemoglobin and Gγ to Aγ ratios in mediterranean patients with thalassemia minor and majorAmerican Journal of Hematology, 1985
- Five haplotypes in Black β-thalassaemia heterozygotes: three are associated with high and two with lowGγ values in fetal haemoglobinBritish Journal of Haematology, 1985
- High Performance Liquid Cbromatographic Separation of Globin Chains on a Large-Pore C4ColumnJournal of Liquid Chromatography, 1984
- beta-Thalassemia in American Blacks: novel mutations in the "TATA" box and an acceptor splice site.Proceedings of the National Academy of Sciences, 1984
- Construction of Human Gene Libraries from Small Amounts cf Peripheral Blood: Analysis of β-Like Globin GenesHemoglobin, 1981
- DNA sequencing with chain-terminating inhibitorsProceedings of the National Academy of Sciences, 1977
- Further Nodification of the Mtcrochromatographic Deternination of Hemoglobin AHemoglobin, 1977
- Estimation of Small Percentages of Fœtal HæmoglobinNature, 1959