Georgina W. Hall

Nonsense codon mutations in the terminal exon of the beta-globin gene are not associated with a reduction in beta-mRNA accumulation: a mechanism for the phenotype of dominant beta-thalassemia.

S. Thein, G. Hall, Georgina W. Hall, 1994, Blood.

A base substitution (T→C) in codon 29 of the α2‐globin gene causes α thalassaemia

D. Higgs, J. Traeger-Synodinos, E. Kanavakis, 1993 .

Unusually Severe Heterozygous β-Thalassemia: Evidence for an Interacting Gene Affecting Globin Translation

S. Thein, S. Watt, Wood Wg, 1998 .