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B Serjeant

Showing results (11-20 of 16) with videos related to

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Hemoglobin|January 1, 1982
Sickle cell-hemoglobin D Iran: benign sickle cell syndromeB Serjeant, E Myerscough, G R Serjeant, et al.
British Journal of Haematology|June 1, 1993
The clinical significance of serum transferrin receptor levels in sickle cell diseaseA Singhal, J D Cook, B S Skikne, et al.
British Journal of Haematology|August 1, 1983
A trial of folate supplementation in children with homozygous sickle cell diseaseL M Rabb, Y Grandison, K Mason, et al.
Clinical and Laboratory Haematology|January 1, 1991
The red cell distribution width in sickle cell disease--is it of clinical value?M Thame, Y Grandison, K Mason, et al.
British Journal of Haematology|January 1, 1996
Determinants of haemoglobin level in steady-state homozygous sickle cell diseaseG Serjeant, B Serjeant, A Stephens, et al.
British Journal of Haematology|March 1, 1991
The haematology of homozygous sickle cell disease after the age of 40 yearsJ Morris, D Dunn, M Beckford, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Hemoglobin|January 1, 1982
Sickle cell-hemoglobin D Iran: benign sickle cell syndromeB Serjeant, E Myerscough, G R Serjeant, et al.
British Journal of Haematology|June 1, 1993
The clinical significance of serum transferrin receptor levels in sickle cell diseaseA Singhal, J D Cook, B S Skikne, et al.
British Journal of Haematology|August 1, 1983
A trial of folate supplementation in children with homozygous sickle cell diseaseL M Rabb, Y Grandison, K Mason, et al.
Clinical and Laboratory Haematology|January 1, 1991
The red cell distribution width in sickle cell disease--is it of clinical value?M Thame, Y Grandison, K Mason, et al.
British Journal of Haematology|January 1, 1996
Determinants of haemoglobin level in steady-state homozygous sickle cell diseaseG Serjeant, B Serjeant, A Stephens, et al.
British Journal of Haematology|March 1, 1991
The haematology of homozygous sickle cell disease after the age of 40 yearsJ Morris, D Dunn, M Beckford, et al.
Pageof 2