The Thalassemia Repository

This publication has 42 references indexed in Scilit:

• The β⁰‐thalassemia in an American black family is due to a single nucleotide substitution in the acceptor splice junction of the second intervening sequence
  American Journal of Hematology, 1986
• Molecular Analysis of Deletion and Nondeletion Hereditary Persistence of Fetal Hemoglobin and Identification of a New Mutation Causing ?-Thalassemia
  Annals of the New York Academy of Sciences, 1985
• Dutch β°‐thalassaemia: a 10 kilobase DNA deletion associated with significant γ‐chain production
  British Journal of Haematology, 1984
• Characterization of the B+-Thalassemia Mutation in a Homozygous Yugoslavian Patient
  Hemoglobin, 1984
• Prenatal Diagnosis of β-Thalassemia
  New England Journal of Medicine, 1983
• Direct detection of the common Mediterranean beta-thalassemia gene with synthetic DNA probes. An alternative approach for prenatal diagnosis.
  Journal of Clinical Investigation, 1983
• Structural study of hemoglobin Knossos, β27 (B9) Ala→Ser
  FEBS Letters, 1982
• ‘Silent’ β-thalassaemia caused by a ‘silent’ β-chain mutant: the pathogenesis of a syndrome of thalassaemia intermedia
  British Journal of Haematology, 1982
• A new nonsense mutation as the molecular basis for β° thalassaemia
  Journal of Molecular Biology, 1982
• β+ Thalassemia: Aberrant splicing results from a single point mutation in an intron
  Cell, 1981