Molecular and hematological studies in a large cohort of α0-thalassemia in northeast Thailand: Data from a single referral center

This publication has 19 references indexed in Scilit:

• Presumptive diagnosis of common haemoglobinopathies in Southeast Asia using a capillary electrophoresis system
  International Journal of Laboratory Hematology, 2011
• Molecular, hematological and clinical aspects of thalassemia major and thalassemia intermedia associated with Hb E-β-thalassemia in Northeast Thailand
  Blood Cells, Molecules, and Diseases, 2009
• Thalassemia intermedia associated with the Hb Constant Spring EE Bart's disease in pregnancy: A molecular and hematological analysis
  Blood Cells, Molecules, and Diseases, 2007
• Prenatal Diagnosis of Hb Bart’s Hydrops Fetalis Caused by a Genetic Compound Heterozygosity for Two Different αo-Thalassemia Determinants
  Fetal Diagnosis and Therapy, 2007
• α⁰-Thalassemia and Related Disorders in Northeast Thailand: A Molecular and Hematological Characterization
  Acta Haematologica, 2006
• Development and Application of a Real‐Time Quantitative PCR for Prenatal Detection of Fetal α⁰‐Thalassemia from Maternal Plasma
  Annals of the New York Academy of Sciences, 2006
• α‐Thalassemia: Hb H Disease and Hb Barts Hydrops Fetalis
  Annals of the New York Academy of Sciences, 2005
• A Reliable Screening Protocol for Thalassemia and Hemoglobinopathies in Pregnancy
  American Journal of Clinical Pathology, 2005
• The Diverse Molecular Basis and Hematological Features of Hb H and AEBart’s Diseases in Northeast Thailand
  Acta Haematologica, 2004
• COMPOUND HETEROZYGOSITY FORα⁰-THALASSEMIA (−−^THAI) AND Hb CONSTANT SPRING CAUSES SEVERE Hb H DISEASE
  Hemoglobin, 2002