Molecular characteristics of α+-thalassemia (3.7 kb deletion) in Southeast Asia: Molecular subtypes, haplotypic heterogeneity, multiple founder effects and laboratory diagnostics

This publication has 20 references indexed in Scilit:

• Genetic heterogeneity of hemoglobin AEBart's disease: A large cohort data from a single referral center in northeast Thailand
  Blood Cells, Molecules, and Diseases, 2014
• Micromapping of Thalassemia and Hemoglobinopathies in Diferent Regions of Northeast Thailand and Vientaine, Laos People's Democratic Republic
  Hemoglobin, 2011
• Hemoglobin Q-Thailand related disorders: Origin, molecular, hematological and diagnostic aspects
  Blood Cells, Molecules, and Diseases, 2010
• Prevention of severe thalassemia in northeast Thailand: 16 years of experience at a single university center
  Prenatal Diagnosis, 2010
• The global problem of genetic disease
  Annals of Human Biology, 2005
• The Diverse Molecular Basis and Hematological Features of Hb H and AEBart’s Diseases in Northeast Thailand
  Acta Haematologica, 2004
• Rapid analysis of ‐α^3.7 thalassaemia and ααα^{anti 3.7} triplication by enzymatic amplification analysis
  British Journal of Haematology, 1993
• Molecular Characterization of Hb H Disease by Polymerase Chain Reaction
  Acta Haematologica, 1993
• Alpha-thalassemia in Papua New Guinea
  Human Genetics, 1986
• Independent recombination events between the duplicated human α globin genes; implications for their concerted evolution
  Nucleic Acids Research, 1984