Next‐generation sequencing as a tool for breakpoint analysis in rearrangements of the globin gene clusters von Clark, B. E., Shooter, C., Smith, F., Brawand, D., Thein, S. L.

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Genetic influences on F cells and other hematologic variables : a twin heritability study von GARNER, C, TATU, T, REITTIE, J. E, LITTLEWOOD, T, DARLEY, J, CERVINO, S, FARRALL, M, KELLY, P, SPECTOR, T. D, THEIN, S. L

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Control of fetal hemoglobin: new insights emerging from genomics and clinical implications von Thein, Swee Lay, Menzel, Stephan, Lathrop, Mark, Garner, Chad

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Pulmonary function abnormalities in children with sickle cell disease von Sylvester, K P, Patey, R A, Milligan, P, Dick, M, Rafferty, G F, Rees, D, Thein, S L, Greenough, A

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Molecular diagnosis of haemoglobin disorders von Clark, B. E., Thein, S. L.

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IS IT DOMINANTLY INHERITED β THALASSAEMIA OR JUST A β‐CHAIN VARIANT THAT IS HIGHLY UNSTABLE? von Thein, Swee Lay

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Beta‐thalassaemia intermedia: is it possible consistently to predict phenotype from genotype? von HO, P. J, HALL, G. W, LUO, L. Y, WEATHERALL, D. J, THEIN, S. L

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Computed tomography and pulmonary function abnormalities in sickle cell disease von Sylvester, K. P, Desai, S. R, Wells, A. U, Hansell, D. M, Awogbade, M, Thein, S. L, Greenough, A

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Haplotype Mapping of a Major Quantitative-Trait Locus for Fetal Hemoglobin Production, on Chromosome 6q23 von Garner, C., Mitchell, J., Hatzis, T., Reittie, J., Farrall, M., Thein, S.L.

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Venous thromboembolism in adults with sickle cell disease: experience of a single centre in the UK von van Hamel Parsons, V., Gardner, K, Patel, R, Thein, S L

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Fetal hemoglobin levels in adults von Rochette, J., Craig, J.E., Thein, S.L.

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The haematology of Jamaicans: red cell indices in HbAA, HbAS, HbAC, and HbA-HPFH genotypes von Serjeant, G. R., Serjeant, B. E., Mason, K. P., Gibson, F., Osmond, C., Thein, S. L., Happich, M., Kulozik, A. E.

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Individual-specific 'fingerprints' of human DNA von Jeffreys, A. J, Wilson, V, Thein, S. L

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Peak expiratory flow in Afro-Caribbean children with and without sickle cell anaemia von Sylvester, KP, Patey, RA, Rafferty, GF, Rees, D, Thein, SL, Greenough, A

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Treatment of thalassaemia major with phenylbutyrate and hydroxyurea von Olivieri, Nancy F, Rees, David C, Ginder, Gordon D, Thein, Swee Lay, Brittenham, Gary M, Waye, John S, Weatherall, DJ

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Gene regulation and deregulation: a β globin perspective von Ho, P.Joy, Thein, S.L.

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Alpha-thalassaemia trait as a cause of unexplained microcytosis in a South African population von Loonat, Sakina Bibi, Naran, Nitien Hira, Thein, Swee Lay, Alli, Nazeer Ahmed

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PS-208 Genetic Predisposition To The Development Of Bronchopulmonary Dysplasia In Infants Born Prematurely von May, CA, Best, S, Peacock, J, Thein, SL, Greenough, A

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Molecular Basis for Dominantly Inherited Inclusion Body β-Thalassemia von Thein, S. L., Hesketh, C., Taylor, P., Temperley, I. J., Hutchinson, R. M., Old, J. M., Wood, W. G., Clegg, J. B., Weatherall, D. J.

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Determinants of iron status and bilirubin levels in congenital dyserythropoietic anaemia type I von WICKRAMASINGHE, S. N, THEIN, S. L, SRICHAIRATANAKOOL, S, PORTER, J. B

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