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Pathologie-Biologie|March 19, 1999
[Molecular and cellular pathophysiology of sickle cell anemia]D Labie, J Elion
Annales De Biologie Clinique|January 1, 1981
[Recent data concerning abnormal hemoglobins (author's transl)]D Labie, J Elion
Medecine Tropicale : Revue Du Corps De Sante Colonial|April 28, 2011
[The problem of sickle cell disease in Africa]D Labie, J Elion
Thrombosis and Haemostasis|February 29, 1976
Isolation of preliminary characterization of a vitamin K dependent peptide from human prothrombinJ Elion, R Benarous, D Labie
Biochimie|January 1, 1976
Ca++ binding properties of human prothrombinR Benarous, J Elion, D Labie
Current Opinion in Hematology|March 24, 1999
Long-term hydroxyurea treatment in young sickle cell patientsM Maier-Redelsperger, D Labie, J Elion
European Journal of Biochemistry|April 1, 1986
Differences in DNase I sensitivity and methylation within the human beta-globin gene domain and correlation with expressionC Arapinis, J Elion, D Labie, et al.
British Journal of Haematology|September 1, 1982
Homozygous deletional alpha + thalassaemia associated with unequal expression of the two remaining alpha 1 genes (alpha 1A and alpha 1Q)J Pagnier, J Elion, C Lapouméroulie, et al.
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