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Lancet (London, England)|October 28, 1995
World distribution of factor V LeidenD C Rees, M Cox, J B CleggBlood|September 10, 1998
Is hemoglobin instability important in the interaction between hemoglobin E and beta thalassemia?D C Rees, J B Clegg, D J WeatherallBlood|November 11, 1999
Why are hemoglobin F levels increased in HbE/beta thalassemia?D C Rees, J B Porter, J B Clegg, et al.British Journal of Haematology|March 1, 1996
Evidence for a single origin of factor V LeidenM J Cox, D C Rees, J J Martinson, et al.Annals of the New York Academy of Sciences|July 21, 1998
The hemoglobin E syndromesD C Rees, L Styles, E P Vichinsky, et al.British Journal of Haematology|November 25, 1998
Alpha thalassaemia is associated with increased soluble transferrin receptor levelsD C Rees, T N Williams, K Maitland, et al.Nature Genetics|May 1, 1997
Global distribution of the CCR5 gene 32-basepair deletionJ J Martinson, N H Chapman, D C Rees, et al.British Journal of Haematology|May 8, 1999
Born to clot: the European burdenD C Rees, N H Chapman, M T Webster, et al.Blood|October 1, 1996
Interaction of hemoglobin E and pyrimidine 5' nucleotidase deficiencyD C Rees, J Duley, H A Simmonds, et al.The American Journal of Tropical Medicine and Hygiene|May 27, 1999
Reduced soluble transferrin receptor concentrations in acute malaria in VanuatuT N Williams, K Maitland, D C Rees, et al.Pageof 257