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British Journal of Haematology|February 1, 1975
A form of hereditary persistence of fetal haemoglobin characterized by uneven cellular distribution of haemoglobin F and the production of haemoglobins A and A2 in homozygotesD J Weatherall, R Cartner, J B Clegg, et al.
British Journal of Haematology|December 1, 1988
The interaction of alpha thalassaemia and sickle cell-beta zero thalassaemiaP Vyas, D R Higgs, D J Weatherall, et al.
The Journal of Experimental Medicine|April 1, 1991
Surface antigen expression on Plasmodium falciparum-infected erythrocytes is modified in alpha- and beta-thalassemiaG A Luzzi, A H Merry, C I Newbold, et al.
American Journal of Human Genetics|May 1, 1987
Polynesian origins and affinities: globin gene variants in eastern PolynesiaA V Hill, B Gentile, J M Bonnardot, et al.
Nucleic Acids Research|October 11, 1982
Multiple arrangements of the human embryonic zeta globin genesP Winichagoon, D R Higgs, S E Goodbourn, et al.
American Journal of Human Genetics|September 1, 1990
The molecular basis of beta-thalassemia in Thailand: application to prenatal diagnosisS L Thein, P Winichagoon, C Hesketh, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1975
Human globin gene analysis for a patient with beta-o/delta beta-thalassemiaS Ottolenghi, W G Lanyon, R Williamson, et al.
American Journal of Human Genetics|February 1, 1994
Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiersS L Thein, M Sampietro, K Rohde, et al.
British Journal of Haematology|November 1, 1980
The genetic basis of Hb Q-H diseaseD R Higgs, D M Hunt, H C Drysdale, et al.
The New England Journal of Medicine|December 11, 1980
A new genetic basis for hemoglobin-H diseaseL Pressley, D R Higgs, J B Clegg, et al.
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