REFERENCES
- Liu Y. T., Old J. M., Miles K., Fisher C. A., Weatherell D. J., Clegg J. B. Rapid Detection of α-Thalassaemia Deletions and α-Globin Gene Triplication by Multiplex Polymerase Chain Reaction. Br. J. Haematol. 2000; 108(2)295–299
- Chang J. G., Chen P. H., Chiou S. S., Lee L. S., Perng L. I., Liu T. C. Rapid Diagnosis of β-Thalassemia Mutations in Chinese by Naturally and Amplified Created Restriction Sites. Blood 1992; 80(8)2092–2096
- Chang J. G., Shih M-C., Liu S-C., Peng C-T. Hb Manitoba in Taiwanese: a C→A Substitution at Codon 102 of the α2-Globin Gene. Hemoglobin 2001; 25(4)437–439
- Chang J. G., Yang T-Y., Perng L-I., Wang N-M., Peng C-T., Tsai C-H. Hb Siriraj: a G→A Substitution at Codon 7 of the β-Globin Chain Creates an MboII Cutting Site. Hemoglobin 1999; 23(2)197–199
- Vella F., Ager J.A. M., Lehmann H. An Abnormal Hemoglobin in a Chinese: Haemoglobin G. Nature 1958; 182: 460–461
- Liu T-C., Yen J-S., Shen J-S., Chen Y-H., Lee L. S., Chen P-H., Chang J-G. Rapid Molecular Diagnosis of Hemoglobin Variants by RT-PCR of Reticulocyte mRNA and Direct Sequencing. Hemoglobin 1992; 16(5)379–388