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Southern Medical Journal|February 1, 1983
Hemophilic splenic rupture without thrombocytosisJ S Krauss, D A HahnClinical Chemistry|October 1, 1985
Estimation of highly increased concentrations of fetal hemoglobin in Fanconi's anemiaJ S Krauss, D A Hahn, M H Jonah, et al.Annals of Clinical and Laboratory Science|September 1, 1987
The affinity glycated hemoglobin in a family with hereditary spherocytosis and in other non-hemoglobinopathic hemolytic anemiasJ S Krauss, D A Hahn, D Harper, et al.Southern Medical Journal|September 1, 1986
Automated leukocyte differentials in trisomy 13R A Bradley, J L Newsome, J S Krauss, et al.Annals of Clinical and Laboratory Science|October 25, 2000
The proportion of hybrid heterodimers in homozygous or doubly heterozygous beta chain variant hemoglobinopathies associated with alpha chain hemoglobin variantsJ S KraussDrug Intelligence & Clinical Pharmacy|June 1, 1983
Hexamethylmelamine and pentamethylmelamine: an updateD A HahnSouthern Medical Journal|November 1, 1979
Miliary tuberculosis and consumption of clotting factors by multifocal vasculopathic coagulationJ S Krauss, D H WalkerObstetrics and Gynecology|March 1, 1986
Indirect antiglobulin test and anti-D prophylaxis in hereditary persistence of fetal hemoglobinH E Fadel, J S KraussAnnals of Clinical and Laboratory Science|January 1, 1990
A comparison of two macroscopic platelet agglutination assays for von Willebrand factorR D Wright, J S KraussPageof 5