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Annals of Clinical and Laboratory Science|July 1, 1986
The selective suppression of immunogenicity by hyaluronic acidJ M Delmage, D R Powars, P K Jaynes, et al.Seminars in Hematology|July 1, 1991
Sickle cell anemia: beta s-gene-cluster haplotypes as prognostic indicators of vital organ failureD R PowarsHematology/Oncology Clinics of North America|June 1, 1991
Beta s-gene-cluster haplotypes in sickle cell anemia. Clinical and hematologic featuresD R PowarsClinical Pediatrics|February 1, 1990
Sickle cell disease. Summer camp. Experience of a 22-year community-supported programD R Powars, M BrownProgress in Clinical and Biological Research|January 1, 1987
Is sickle cell crisis a valid measure of clinical severity in sickle cell anemia?D R Powars, L S ChanAnnals of Clinical and Laboratory Science|January 1, 1985
Glycosaminoglycan in the blood and renal tissue of a patient with nephroblastomatosisP K Jaynes, S E AllertonAnnals of the New York Academy of Sciences|January 1, 1989
The influence of fetal hemoglobin on the clinical expression of sickle cell anemiaD R Powars, L Chan, W A SchroederThe American Journal of Pediatric Hematology/Oncology|January 1, 1990
Beta S-gene-cluster haplotypes in sickle cell anemia: clinical implicationsD R Powars, L Chan, W A SchroederPageof 5