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

This publication has 92 references indexed in Scilit:

• 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
• A NOVEL β‐THALASSAEMIA MUTATION: DELETION OF 4 bp (–AAAC) IN THE 5’TRANSCRIPTIONAL SEQUENCE
  British Journal of Haematology, 1991
• Molecular heterogeneity of β‐thalassaemia in the Japanese: identification of two novel mutations
  British Journal of Haematology, 1990
• β-Thalassemia Intermedia in Two Turkish Families is Caused by the Interaction of HB Knossos [β27(B9)ALA→SER] and of HB City of hope [β69(E13)Gly→Ser] with B°-Thalassemia
  Hemoglobin, 1989
• β-thalassemia due to A T→A mutation within the ATA box
  Biochemical and Biophysical Research Communications, 1988
• The Thalassemia Repository
  Hemoglobin, 1987
• 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