Rapid detection and prenatal diagnosis of β-thalassaemia: studies in Indian and Cypriot populations in the UK

This publication has 10 references indexed in Scilit:

• Detection of specific DNA sequences by fluorescence amplification: a color complementation assay.
  Proceedings of the National Academy of Sciences, 1989
• AMPLIFICATION REFRACTORY MUTATION SYSTEM FOR PRENATAL DIAGNOSIS AND CARRIER ASSESSMENT IN CYSTIC FIBROSIS
  The Lancet, 1989
• Molecular characterization of a high A2 beta thalassemia by direct sequencing of single strand enriched amplified genomic DNA
  Blood, 1989
• Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)
  Nucleic Acids Research, 1989
• Hinf I polymorphism 3′ to the human β-globin gene detected by the polymerase chain reaction (PCR)
  Nucleic Acids Research, 1989
• Direct sequencing from low-melt agarose with Sequenase@
  Nucleic Acids Research, 1989
• Rapid and non‐radioactive prenatal diagnosis of β thalassaemia and sickle cell disease: application of the polymerase chain reaction (PCR)
  British Journal of Haematology, 1988
• The molecular basis of thalassaemia major and thalassaemia intermedia in Asian Indians: application to prenatal diagnosis
  British Journal of Haematology, 1988
• Diagnosis of Sickle Cell Anemia and β-Thalassemia with Enzymatically Amplified DNA and Nonradioactive Allele-Specific Oligonucleotide Probes
  New England Journal of Medicine, 1988
• Analysis of enzymatically amplified β-globin and HLA-DQα DNA with allele-specific oligonucleotide probes
  Nature, 1986