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Hemeteam is a collection of topics designed to provide basic principles used in solving common hematological problems. It is targeted to students and residents, and person wanting a review. MCQs with instant feedback are provided for self -assessment. I hope you find this useful. Suggestions and comments are welcome. Please send your e-mail address if you want a reply. HemeTeam is supported by internet explorer 4.0 and higher, and Netscape 4.x BUT NOT Netscape 6.x
Hemeteam.com ~
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ASCAA, American Sickle Cell Anemia Association, ASCAA, Sickle Cell, Sickle, Cell
Beta Thal, Trait, Anemia, Delta beta thal, Alpha Thalassemia, gene, hereditary persistent fetal hemoglobin, Sickle cell trait, Sickle cell trait alpha thal, sickle cell anemia, cord blood, sickle c, sickle d, sickle e, sickle g, sickle j, sickle j, sickle lepore, disease, sickle n, sickle o, homozygous c, HB c trait, HB c harlem trait, HB c trait alpha, HB e trait, HB j trait, HB lepore trait, HB n trait, HB o trait, HB S, dna, abnormal cells, hemoglobin, hemoglobin cells, hemoglobin a, disease, newborn screening, supportive services, inherited disease, red blood cells, sickle shape, anemia, capillaries, educational materials, variants, protein-iron, blood cessels, abnormality, Dr. James Bryan Herrick, 1910,genetic makeup, research, family support, counseling, teen education, family counseling, teen counseling, Cleveland Clinic Foundation, Bioethics, Blood Disorder, Cell, Hematology, Morphine, Sickle Cell Disease, Blood Vessel, Saharan Africa, 1 in every 500 African-American, defective gene, Delayed growth, Infections, Stroke, Acute chest syndrome, intravenous fluids, hydroxyurea, Bone marrow transplantation
ASCAA
Ascaa.org ~
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