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Pathologie-Biologie|March 19, 1999
[Molecular and cellular pathophysiology of sickle cell anemia]D Labie, J ElionAnnales De Biologie Clinique|January 1, 1981
[Recent data concerning abnormal hemoglobins (author's transl)]D Labie, J ElionMedecine Tropicale : Revue Du Corps De Sante Colonial|April 28, 2011
[The problem of sickle cell disease in Africa]D Labie, J ElionClinica Chimica Acta; International Journal of Clinical Chemistry|February 15, 1979
Quantitation of hemoglobin A1c: a rapid, automated precision-chromatography techniqueH Wajcman, B Dastugue, D LabieThrombosis and Haemostasis|February 29, 1976
Isolation of preliminary characterization of a vitamin K dependent peptide from human prothrombinJ Elion, R Benarous, D LabieHuman Genetics|June 9, 1978
Genetic and biosynthetic studies of families carrying hemoglobin J alpha Mexico: association of alpha-thalassemia with HbJG Trabuchet, M Benabadji, D LabieClinica Chimica Acta; International Journal of Clinical Chemistry|June 1, 1976
Isoelectrofocusing: a method of multiple applications for hemoglobin studiesR Krishnamoorthy, H Wajcman, D LabieLa Nouvelle Presse Medicale|May 12, 1979
[Glycosylated hemoglobin: résults of 550 cases (author's transl)]H Wajcman, B Dastugue, D LabieAnnales De Genetique|January 1, 1988
Types of alpha+ thalassemia in Southeast Asia refugeesC Dodé, D Labie, J RochettePageof 20