The molecular basis for the thalassaemias in Sri Lanka

This publication has 16 references indexed in Scilit:

• A NOVEL β⁰-THALASSEMIA MUTATION AT CODON 55 (−A) AND A RARE 17 bp DELETION AT CODONS 126–131 IN THE INDIAN POPULATION
  Hemoglobin, 2002
• A MULTI-CENTER STUDY IN ORDER TO FURTHER DEFINE THE MOLECULAR BASIS OF β-THALASSEMIA IN THAILAND, PAKISTAN, SRI LANKA, MAURITIUS, SYRIA, AND INDIA, AND TO DEVELOP A SIMPLE MOLECULAR DIAGNOSTIC STRATEGY BY AMPLIFICATION REFRACTORY MUTATION SYSTEM-POLYMERASE CHAIN REACTION
  Hemoglobin, 2001
• The association of Hb khartoum [β124(H2)Pro→Arg] with γ⁺-thalassemia is responsible for hemolytic disease in the newborn of a sudanese family
  Hemoglobin, 1999
• The spectrum of β‐thalassaemia mutations on the Indian subcontinent: the basis for prenatal diagnosis
  British Journal of Haematology, 1991
• Hemoglobinopathies in sri Lanka and Their Anthropological Implications
  Hemoglobin, 1989
• THE MUTATION AND POLYMORPHISM OF THE HUMAN β-GLOBIN GENE AND ITS SURROUNDING DNA
  Annual Review of Genetics, 1984
• Thalassaemia in Ceylon
  Acta Haematologica, 1967
• Sinhalese Family with Haemoglobin S
  BMJ, 1962
• Haemoglobin E Syndromes in a Ceylonese Family
  BMJ, 1958
• Cooley's Anaemia in Sinhalese Children
  Archives of Disease in Childhood, 1951