Rapid diagnosis of β thalassemia mutations in mediterraneans by PCR and restriction analysis of natural or created sites
- 31 July 1997
- journal article
- Published by Elsevier in Clinical Biochemistry
- Vol. 30 (5), 433-437
- https://doi.org/10.1016/s0009-9120(97)00044-1
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Rapid diagnosis of beta-thalassemia mutations in Chinese by naturally and amplified created restriction sitesBlood, 1992
- RAPID DETECTION OF A MEDITERRANEAN β° SPLICE JUNCTION MUTATION BY DNA AMPLIFICATION AND BsaB1 MAPPINGBritish Journal of Haematology, 1990
- 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
- Prenatal diagnosis of beta thalassaemia based on restriction endonuclease analysis of amplified fetal DNA.Journal of Medical Genetics, 1989
- β THALASSAEMIA MUTATIONS IN MEDITERRANEAN POPULATIONSBritish Journal of Haematology, 1989
- Modification of enzymatic-ally amplified DNA for the detection of point mutationsNucleic Acids Research, 1989
- Molecular basis and prenatal diagnosis of beta-thalassemiaBlood, 1988
- Analysis of enzymatically amplified β-globin and HLA-DQα DNA with allele-specific oligonucleotide probesNature, 1986
- DIRECT DETECTION OF β°39 THALASSAEMIC MUTATION WITH Mae 1The Lancet, 1985
- A β-thalassemia ledon abolishes the sameMstII site as the sickle mutationNucleic Acids Research, 1983