The detection of β-globin gene mutations in β-thalassemia using oligonucleotide probes and amplified DNA

This publication has 16 references indexed in Scilit:

• Analysis of enzymatically amplified β-globin and HLA-DQα DNA with allele-specific oligonucleotide probes
  Nature, 1986
• Use of oligonucleotide hybridization in the characterization of a beta zero-thalassemia gene (beta 37 TGG----TGA) in a Saudi Arabian family [published erratum appears in Blood 1986 Jul;68(1):323]
  Blood, 1986
• Haplotypes of β^SChromosomes Among Patients with Sickle Cell Anemia from Georgia
  Hemoglobin, 1986
• The Thalassemia Repository
  Hemoglobin, 1986
• DIRECT DETECTION OF β°39 THALASSAEMIC MUTATION WITH Mae 1
  The Lancet, 1985
• Five haplotypes in Black β-thalassaemia heterozygotes: three are associated with high and two with lowGγ values in fetal haemoglobin
  British Journal of Haematology, 1985
• Direct detection of the common Mediterranean beta-thalassemia gene with synthetic DNA probes. An alternative approach for prenatal diagnosis.
  Journal of Clinical Investigation, 1983
• A β-thalassemia ledon abolishes the sameMstII site as the sickle mutation
  Nucleic Acids Research, 1983
• Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster
  Nature, 1982
• Construction of Human Gene Libraries from Small Amounts cf Peripheral Blood: Analysis of β-Like Globin Genes
  Hemoglobin, 1981