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American Journal of Clinical Pathology|January 1, 1981
Prevalence of alpha-chain variants at birthO Castro, W P Winter, T C Lee, et al.American Journal of Hematology|January 1, 1981
Freeze preservation of sickle erythrocytesO Castro, K P Hardy, W P Winter, et al.Texas Reports on Biology and Medicine|January 1, 1980
Geographic and ethnic distribution of human hemoglobin variantsW P WinterAmerican Journal of Hematology|February 1, 1993
G gamma A gamma (beta+) hereditary persistence of fetal hemoglobin: the G gamma -158 C-->T mutation in cis to the -175 T-->C mutation of the A gamma-globin gene results in increased G gamma-globin synthesisM B Coleman, J G Adams, M H Steinberg, et al.Journal of the National Medical Association|October 29, 2000
Automated oxyhemoglobin dissociation curve construction to assess sickle cell anemia therapyR C Young, R E Rachal, M Del Pilar Aguinaga, et al.Journal of the National Medical Association|February 1, 1981
Use of citrate agar electrophoresis in evaluation of antisickling agentsE Wilson, W P WinterScience (New York, N.Y.)|July 8, 1983
Interaction of human hemoglobin and its variants with agarW P Winter, J YodhHematology/Oncology Clinics of North America|December 1, 1996
Systemic fat embolism and pulmonary hypertension in sickle cell diseaseO CastroSouthern Medical Journal|March 1, 1981
Sickle cell thalassemia, thrombocytosis, and erythrocytosisO CastroPageof 26