The β- and δ-Thalassemia Repository (Eighth Edition)

This publication has 109 references indexed in Scilit:

• Initiation codon mutation (ATG → ATA) of the β‐globin gene causing β‐thalassemia in a Swedish family
  American Journal of Hematology, 1995
• A novel β‐thalassaemia mutation in the 5’untranslated region of the β‐globin gene
  British Journal of Haematology, 1994
• Molecular characterization of ?-thalassemia in Hungary
  Human Genetics, 1993
• Molecular characterisation of Vietnamese HPFH
  Human Mutation, 1993
• A novel β-thalassemia mutation (G→A) at the initiation codon of the β-globin gene
  Human Mutation, 1992
• Compound heterozygosity for a β∘-thalassemia (frameshift codons 38/39; -C) and a nondeletional swiss type of HPFH (A→C at NT -110, Gγ) in a Czechoslovakian family
  Annals of Hematology, 1991
• A novel δº mutation in cis with Hb Knossos: a study of different genetic interactions in three Egyptian families
  British Journal of Haematology, 1991
• β Thalassemia due to a novel mutation in IVS 1 sequence donor site consensus sequence creating a restriction site
  Biochemical and Biophysical Research Communications, 1986
• 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
• Dutch β°‐thalassaemia: a 10 kilobase DNA deletion associated with significant γ‐chain production
  British Journal of Haematology, 1984