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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.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|March 1, 1986
Feasibility of prenatal diagnosis of beta thalassaemia by DNA polymorphisms in an Italian populationJ S Wainscoat, S Work, M Sampietro, 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.Cell|May 1, 1979
The molecular basis of alpha-thalassemias: frequent occurrence of dysfunctional alpha loci among non-Asians with Hb H diseaseS H Orkin, J Old, H Lazarus, et al.Pageof 28