Polymerase chain reaction amplification applied to the determination of β‐like globin gene cluster haplotypes
- 1 September 1989
- journal article
- research article
- Published by Wiley in American Journal of Hematology
- Vol. 32 (1) , 66-69
- https://doi.org/10.1002/ajh.2830320113
Abstract
We report here on the application of the polymerase chain reaction (PCR) technique for the determination of the β-like gene cluster haplotypes. Seven fragments containing each one of the following polymorphic sites—Xmnl 5′ to the Gγ gene, Hindlll in the IVSII of Gγ and A γ gene, Hincll 3′ and inside the γ gene, Hinfl 5′ of the β gene—and Hpal 3′ of the β gene—are amplified using the PCR technique. Each amplified fragment is subsequently digested with the appropriate enzyme, analyzed by electrophoresis on agarose gel containing ethidium bromide, and visualized under ultraviolet light. This technique has the advantages of rapidity, safety, and cost-effectiveness.Keywords
This publication has 10 references indexed in Scilit:
- Detection of specific sequences among DNA fragments separated by gel electrophoresisPublished by Elsevier ,2006
- Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA PolymeraseScience, 1988
- THE HEMATOLOGIC CHARACTERISTICS OF SICKLE-CELL-ANEMIA BEARING THE BANTU HAPLOTYPE - THE RELATIONSHIP BETWEEN G-GAMMA AND HBF LEVEL1987
- The hematologic characteristics of sickle cell anemia bearing the Bantu haplotype: the relationship between G gamma and HbF levelBlood, 1987
- Molecular Analysis of the High-Hemoglobin-F Phenotype in Saudi Arabian Sickle Cell AnemiaNew England Journal of Medicine, 1987
- GEOGRAPHICAL SURVEY OF BETA-S-GLOBIN GENE HAPLOTYPES - EVIDENCE FOR AN INDEPENDENT ASIAN ORIGIN OF THE SICKLE-CELL MUTATION1986
- Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell AnemiaScience, 1985
- Hematologically and Genetically Distinct Forms of Sickle Cell Anemia in AfricaNew England Journal of Medicine, 1985
- Evidence for the multicentric origin of the sickle cell hemoglobin gene in Africa.Proceedings of the National Academy of Sciences, 1984
- Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene clusterNature, 1982