1. Molecular characterisation of a high A2 P thalassemia by direct sequencing of single strand enriched amplified deleted.3637 The mechanism(s) by which sequences in the 5' f globin gene might influence genomic DNA;Thein, S.L.; Hesketh, C.; Brown, J.M.; Anstey, A.V.; Weatherall, D.J.;Blood,1989
2. A f3- thalassemia gene caused by a 290-base pair deletion: the 6 and y globin gene expression have not been fully elucidated. Deletions removing the analysis by direct sequencing of enzymatically amplified DNA;Spiegelberg, R.; Aulehla-Scholz, C.; Erlich, H.; Horst, J.;Blood,1989
3. Characterisation of the breakpoint of a 3-5 kb deletion of the I-globin gene. Genomics 1991; 10: 509-11. tion of the 6 globin gene. If this were the mechanism for the raised Hb A2 it should;Lynch, JR, Brown; JM, Best; S, Jennings; MW, Weatherall; D.J.
4. Australian 0°-thalassaemia: a high Hb AR?0-thalassaemia due to a 12 kb deletion commencing 5 to the f-globin gene Alternatively it has been suggested that the transcription of the 6 globin gene promoter cluster;Motum, P.I.; Lindeman, R.; Hamilton, T.J.; Trent, R.J.;Br J Haematol,1992
5. Different 3' end points of deletions causing 6benhancer.5 Enhancers have been identified thalassemia and hereditary persistence of fetal hemoglodownstream from the A'y3";Tuan, D.; Feingold, E.; Newman, M.; Weissman, S.M.; Forget, B.G.,1983