The Thalassemia Repository (Ninth Edition; Part II)

This publication has 108 references indexed in Scilit:

• The Australian type of nondeletional ^Gγ‐HPFH has a C→G substitution at nucleotide — 114 of the ^Gγ gene
  British Journal of Haematology, 1994
• Molecular characterisation of Vietnamese HPFH
  Human Mutation, 1993
• 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
• The DNA deletion in an Indian δβ‐thalassaemia begins one kilobase from the ^Aγ globin gene and ends in an LI repetitive sequence
  British Journal of Haematology, 1989
• Two New Large Deletions Resulting in εγδβ-Thalassemia
  Acta Haematologica, 1988
• (^Aγδβ)°‐Thalassaemia in Blacks is due to a deletion of 34 kbp of DNA
  British Journal of Haematology, 1985
• Hemolytic disease of the newborn caused by a new deletion of the entire beta-globin cluster.
  Journal of Clinical Investigation, 1983
• Heterogeneity in the molecular basis of hereditary persistence of fetal haemoglobin
  Nature, 1980
• Deletion of the A gamma-globin gene in G gamma-delta beta-thalassemia.
  Journal of Clinical Investigation, 1979
• Application of Endonuclease Mapping to the Analysis and Prenatal Diagnosis of Thalassemias Caused by Globin-Gene Deletion
  New England Journal of Medicine, 1978