Alpha-thalassaemia. by Harteveld, C, Higgs, D

Expression of the human alpha-globin cluster in the absence of the major regulatory element Mcs-R2 by Badat, M, Davies, JOJ, Van Beers, EJ, Harteveld, C, Downes, D, Higgs, DR

A novel deletion causing alpha thalassemia clarifies the importance of the major human alpha globin regulatory element. by Viprakasit, V, Harteveld, C, Ayyub, H, Stanley, J, Giordano, P, Wood, W, Higgs, D

ATR-16 syndrome: mechanisms linking monosomy to phenotype by Babbs, C, Brown, J, Horsley, S, Slater, J, Maifoshie, E, Kumar, S, Ooijevaar, P, Kreik, M, Dixon-Mciver, A, Harteveld, C, Traeger-Synodinos, J, Wilkie, A, Higgs, D, Buckle, V

Beta thalassaemia intermedia due to co-inheritance of three unique alpha globin cluster duplications characterised by next generation sequencing analysis by Clark, B, Shooter, C, Smith, F, Brawand, D, Steedman, L, Oakley, M, Rushton, P, Rooks, H, Wang, X, Drousiotou, A, Kyrri, A, Hadjigavriel, M, Will, A, Fisher, C, Higgs, D, Phylipsen, M, Harteveld, C, Kleanthous, M, Thein, S

Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach by Giardine, B, Borg, J, Higgs, D, Peterson, K, Philipsen, S, Maglott, D, Singleton, B, Anstee, D, Basak, A, Clark, B, Costa, F, Faustino, P, Fedosyuk, H, Felice, A, Francina, A, Galanello, R, Gallivan, M, Georgitsi, M, Gibbons, R, Giordano, P, Harteveld, C, Hoyer, J, Jarvis, M, Joly, P, Kanavakis, E

Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach. by Giardine, B, Borg, J, Higgs, D, Peterson, K, Philipsen, S, Maglott, D, Singleton, B, Anstee, D, Basak, A, Clark, B, Costa, F, Faustino, P, Fedosyuk, H, Felice, A, Francina, A, Galanello, R, Gallivan, M, Georgitsi, M, Gibbons, R, Giordano, P, Harteveld, C, Hoyer, J, Jarvis, M, Joly, P, Kanavakis, E