Characterization of the breakpoint of a 3.5-kb deletion of the β-globin gene
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[1] D. Weatherall,et al. Rapid detection and prenatal diagnosis of β-thalassaemia: studies in Indian and Cypriot populations in the UK , 1990, The Lancet.
[2] D. Mager,et al. Molecular analysis of deletions in the human beta-globin gene cluster: deletion junctions and locations of breakpoints. , 1990, Genomics.
[3] C. Boehm,et al. Molecular characterization of a beta zero-thalassemia resulting from a 1.4 kilobase deletion. , 1988, Blood.
[4] K. Mullis,et al. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. , 1988, Science.
[5] P. Rowley,et al. Thalassemia: Pathophysiology and management. Part A , 1988 .
[6] M Poncz,et al. Nucleotide sequence analysis of the delta beta-globin gene region in humans. , 1983, The Journal of biological chemistry.