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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.Progress in Clinical and Biological Research|January 1, 1986
The relationship between the common mutations of the alpha gene cluster and its evolutionary historyD J Weatherall, D R Higgs, J B Clegg, et al.British Journal of Haematology|June 20, 1998
Red cell morphology and malaria anaemia in children with Southeast-Asian ovalocytosis band 3 in Papua New GuineaA O'Donnell, S J Allen, C S Mgone, et al.British Journal of Haematology|June 1, 1984
(A gamma delta beta) thalassaemia: similarity of phenotype in four different molecular defects, including one newly describedR J Trent, R W Jones, J B Clegg, et al.British Journal of Haematology|February 26, 2000
Rapid detection of alpha-thalassaemia deletions and alpha-globin gene triplication by multiplex polymerase chain reactionsY T Liu, J M Old, K Miles, et al.Nature|November 24, 1983
Alpha-thalassaemia caused by a polyadenylation signal mutationD R Higgs, S E Goodbourn, J Lamb, et al.Blood|February 1, 1988
The polyadenylation site mutation in the alpha-globin gene clusterS L Thein, R B Wallace, L Pressley, et al.Neurotoxicology and Teratology|May 1, 1987
Effects of intraperitoneal carbon monoxide on fixed-ratio and screen-test performance in the mouseJ S Knisely, D C Rees, J M Salay, et al.Journal of Molecular Biology|July 8, 2000
Structure of a thioredoxin-like [2Fe-2S] ferredoxin from Aquifex aeolicusA P Yeh, C Chatelet, S M Soltis, et al.Pageof 257