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The Journal of Clinical Investigation|June 1, 1984
Hematologic and biosynthetic studies in homozygous hemoglobin Constant SpringS Derry, W G Wood, M Pippard, et al.Human Genetics|February 1, 1988
c-Ha-ras-1 alleles in bladder cancer, Wilms' tumour and malignant melanomaN K Hayward, R Keegan, D J Nancarrow, et al.International Journal of Laboratory Hematology|September 15, 2011
ICSH recommendations for the measurement of haemoglobin FA D Stephens, M Angastiniotis, E Baysal, et al.British Journal of Haematology|October 16, 1999
Role of FcgammaRI (CD64) in erythrocyte elimination and its up-regulation in thalassaemiaE Wiener, D Allen, R J Porter, et al.Clinical Chemistry|April 29, 1998
Prenatal and postnatal diagnoses of thalassemias and hemoglobinopathies by HPLCS Fucharoen, P Winichagoon, R Wisedpanichkij, et al.Blood|May 16, 1998
Membrane phospholipid asymmetry in human thalassemiaF A Kuypers, J Yuan, R A Lewis, et al.Blood|February 1, 1996
Hydroxyurea increases hemoglobin F levels and improves the effectiveness of erythropoiesis in beta-thalassemia/hemoglobin E diseaseS Fucharoen, N Siritanaratkul, P Winichagoon, et al.Hemoglobin|January 17, 2002
A multi-center study in order to further define the molecular basis of beta-thalassemia in Thailand, Pakistan, Sri Lanka, Mauritius, Syria, and India, and to develop a simple molecular diagnostic strategy by amplification refractory mutation system-polymerase chain reactionJ M Old, S N Khan, I Verma, et al.Pageof 27