The mRNA ratios in different forms of α-thalassemia
- 12 April 1996
- journal article
- case report
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
- Vol. 1315 (3) , 188-192
- https://doi.org/10.1016/0925-4439(95)00123-9
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- γ‐mRNA and Hb F levels in β‐thalassaemiaBritish Journal of Haematology, 1994
- The differences in quantities of α2‐and α1‐globin gene variants in heterozygotesBritish Journal of Haematology, 1994
- The relative levels of βA and βS mRNAs in Hb S heterozygotes and in patients with Hb S‐β+ ‐thalassaemia or Hb S‐β+ ‐HPFH combinationsBritish Journal of Haematology, 1994
- Identification of a novel termination codon mutation (TAA-->TAT, Term-- >Tyr) in the alpha 2 globin gene of a Laotian girl with hemoglobin H disease [letter]Blood, 1994
- The -158 (C-->T) promoter mutation is responsible for the increased transcription of the 3' gamma gene in the Atlanta type of hereditary persistence of fetal hemoglobinBlood, 1994
- A PCR‐based strategy to detect the common severe determinants of α thalassaemiaBritish Journal of Haematology, 1992
- High-performance liquid chromatographic separation of human haemoglobinsJournal of Chromatography B: Biomedical Sciences and Applications, 1988
- High Performance Liquid Cbromatographic Separation of Globin Chains on a Large-Pore C4ColumnJournal of Liquid Chromatography, 1984
- Haemoglobin Constant Spring—A Chain Termination Mutant ?Nature, 1971
- Two Haemoglobins Q, α74 (EF3) and α75 (EF4) Aspartic Acid→HistidineBritish Journal of Haematology, 1970