A thalassaemia array for Southeast Asia
- 19 December 2003
- journal article
- Published by Wiley in British Journal of Haematology
- Vol. 124 (2) , 232-239
- https://doi.org/10.1046/j.1365-2141.2003.04758.x
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Detection of mitochondrial single nucleotide polymorphisms using a primer elongation reaction on oligonucleotide microarraysNucleic Acids Research, 2001
- Genetic and Clinical Features of Hemoglobin H Disease in Chinese PatientsNew England Journal of Medicine, 2000
- Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemiaBlood, 2000
- A reverse dot‐blot method for rapid detection of non‐deletion α thalassaemiaBritish Journal of Haematology, 1999
- α‐ and β‐Thalassemia in ThailandAnnals of the New York Academy of Sciences, 1998
- Molecular defects in Hb H hydrops fetalisBritish Journal of Haematology, 1997
- Molecular Diagnostics: Past, present, and futureHuman Mutation, 1993
- Molecular defects in haemophilia B: detection by direct restriction enzyme analysisBritish Journal of Haematology, 1991
- Organization of the ζ‐α genes in ChineseBritish Journal of Haematology, 1986
- Hydrops fetalis due to an unusual form of Hb H diseaseBlood, 1985