References
- Huisman T HJ, Carver M FH, Baysal E. A Syllabus of Thalassemia Mutations (1997). Augusta: The Sickle Cell Anemia Foundation, 1997, http://globin.cse.psu.edu.
- Kueviakoe I, Gerard N, Krishnamoorthy R, Pereira S, Elion J, Ducrocq R. A new high Hb A2-β-thalassemia due to a 468 bp deletion ( − 475 to − 8) in the β-globin gene promoter of the intact β-globin structural gene. Hemoglobin 2004; 28(1):69–72, [PUBMED], [INFOTRIEVE], [CSA]
- Spiegelberg R, Aulehla-Scholz C, Erlich H, Horst J. A β-thalassemia gene caused by a 290-base pair deletion: analysis by direct sequencing of enzymatically amplified DNA. Blood 1989; 73(6):1695–1698, [PUBMED], [INFOTRIEVE], [CSA]
- Waye J S, Eng B, Hunt J A, Chui D HK. Filipino β-thalassemia due to a large deletion: identification of the deletion endpoints and polymerase chain reaction (PCR)-based diagnosis. Hum Genet 1994; 94(5):530–532, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Codrington J F, Li H-W, Kutlar F, Gu L-H, Ramachandran M, Huisman T HJ. Observations on the levels of Hb A2 in patients with different β-thalassemia mutations and a δ-chain variant. Blood 1990; 76(6):1246–1249, [PUBMED], [INFOTRIEVE], [CSA]
- Waye J S, Chui D HK, Eng B, Cai S P, Coleman M B, Adams J G III, Steinberg M H. Hb S/β0-thalassemia due to the ∼ 1.4-kb deletion is associated with a relatively mild phenotype. Am J Hematol 1991; 38(2):108–112, [PUBMED], [INFOTRIEVE], [CSA]
- Waye J S, Cai S P, Eng B, Clark C, Adams J G III, Chui D HK, Steinberg M H. High Hemoglobin A2 β0-thalassemia due to a 532-basepair deletion of the 5′ β-globin gene region. Blood 1991; 77(5):1100–1103, [PUBMED], [INFOTRIEVE], [CSA]