Rapid detection of the highly polymorphic beta globin framework by denaturing gradient gel electrophoresis.
Open Access
- 1 August 1992
- journal article
- Published by BMJ in Journal of Medical Genetics
- Vol. 29 (8) , 574-577
- https://doi.org/10.1136/jmg.29.8.574
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin gene.Journal of Medical Genetics, 1991
- Denaturing gradient gel electrophoresis and direct sequencing of PCR amplified genomic DNA: a rapid and reliable diagnostic approach to beta thalassaemiaBritish Journal of Haematology, 1990
- Use of denaturing gradient gel electrophoresis to detect point mutations in the factor VIII geneGenomics, 1990
- Identification of the multiple beta-thalassemia mutations by denaturing gradient gel electrophoresis.Journal of Clinical Investigation, 1990
- A Novel Frameshift Mutation [FSC 47 (+A)] Causing β-Thalassemia in a Surinam PatientHemoglobin, 1990
- Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reactionGenomics, 1989
- Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.Proceedings of the National Academy of Sciences, 1989
- Mutations in the catalytic domain of human coagulation factor IX: Rapid characterization by direct genomic sequencing of DNA fragments displaying an altered melting behaviorGenomics, 1989
- Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene clusterNature, 1982
- DNA sequence variants in the Gγ-, Aγ-, δ- and β-globin genes of manCell, 1979