Recent publications published by researchers at the MRC WIMM.
The direct antiglobulin test in P. falciparum malaria
Abdalla S. and Weatherall DJ., (1982), British Journal of Haematology, 51, 415 - 425
The interaction of alpha-thalassemia and homozygous sickle-cell disease.
Higgs DR. et al, (1982), N Engl J Med, 306, 1441 - 1446
alpha-globin gene deletions associated with Hb J Tongariki.
Bowden DK. et al, (1982), Br J Haematol, 51, 243 - 249
Inadequacy of Hb Bart's as an indicator of alpha thalassaemia.
Higgs DR. et al, (1982), Br J Haematol, 51, 177 - 178
Limited proteolysis and proton NMR spectroscopy of Bacillus stearothermophilus pyruvate dehydrogenase multienzyme complex.
Duckworth HW. et al, (1982), Eur J Biochem, 124, 63 - 69
Survival and desferrioxamine in thalassaemia major.
Modell B. et al, (1982), Br Med J (Clin Res Ed), 284, 1081 - 1084
The British type of non-deletion HPFH: characterization of developmental changes in vivo and erythroid growth in vitro
Wood WG. et al, (1982), British Journal of Haematology, 50, 401 - 414
alpha-globin gene deletions associated with Hb J Tongariki
Bowden DK. et al, (1982), Br J Haematol, 51, 243 - 249
Sickle cell-hemoglobin D Iran: benign sickle cell syndrome.
Serjeant B. et al, (1982), Hemoglobin, 6, 57 - 59
The clinical and genetic heterogeneity and interactions of the alpha- and beta-thalassemias.
Weatherall DJ. et al, (1982), Birth Defects Orig Artic Ser, 18, 15 - 27
Haemoglobin Synthesis by Fetal Erythroid Cells in an Adult Environment
Bunch C. et al, (1981), British Journal of Haematology, 49, 325 - 336
Highly variable regions of DNA flank the human alpha globin genes.
Higgs DR. et al, (1981), Nucleic Acids Res, 9, 4213 - 4224
Hemoglobin H disease and mental retardation: a new syndrome or a remarkable coincidence?
Weatherall DJ. et al, (1981), N Engl J Med, 305, 607 - 612
A new triplicated alpha-globin gene arrangement in man.
Trent RJ. et al, (1981), Br J Haematol, 49, 149 - 152
Continuous long-term culture of human bone marrow
POTTER CG. et al, (1981), Clinical & Laboratory Haematology, 3, 245 - 255
Genetic and molecular diversity in nondeletion Hb H disease.
Higgs DR. et al, (1981), Proc Natl Acad Sci U S A, 78, 5833 - 5837
Haemoglobin Synthesis in Human Erythroid Bursts during Ontogeny: Reproducibility and Sensitivity to Culture Conditions
Darbre PD. et al, (1981), British Journal of Haematology, 48, 237 - 250
Molecular basis for mild forms of homozygous beta-thalassaemia.
Weatherall DJ. et al, (1981), Lancet, 1, 527 - 529
Alpha thalassemia and homozygous sickle cell disease.
Serjeant GR. et al, (1981), Prog Clin Biol Res, 55, 781 - 788