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An Erythroid Enhancer of BCL11A Subject to Genetic Variation Determines Fetal Hemoglobin Level
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Double heterozygocity for hemoglobin C and beta thalassemia dominant: A rare case of thalassemia intermedia. [PDF]
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An octogenarian with hemoglobin S‐C disease [PDF]
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USE OF CONTINUOUS GLUCOSE MONITORING LEADS TO DIAGNOSIS OF HEMOGLOBIN C TRAIT IN A PATIENT WITH DISCREPANT HEMOGLOBIN A1C AND SELF-MONITORED BLOOD GLUCOSE. [PDF]
AACE Clin Case Rep, 2019 Wright JJ, Hu JR, Shajani-Yi Z, Bao S.
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ARYA Atherosclerosis, 2010 INTRODUCTION: Diabetes is one of the most common endocrine diseases spreading rapidly in the world. Diabetes complications are classified into acute and chronic.
Sedighe Asgary +5 more
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Hybrid formation for liganded hemoglobins A and C at subzero temperatures.
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An A gamma type of nondeletional hereditary persistence of fetal hemoglobin with a T----C mutation at position -175 to the cap site of the A gamma globin gene [PDF]
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Postpartum maternal levels of hemoglobin A1cand cord C-peptide in macrosomic infants of non-diabetic mothers [PDF]
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