Showing results 1 to 5 of 5
Title | Author(s) | Issue Date | Views | |
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2011 | ||||
BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies Journal:Blood Cells, Molecules, and Diseases | 2008 | 134 | ||
Is HbA2 level a reliable diagnostic measurement for β-thalassemia trait in people with iron deficiency? Journal:American Journal of Hematology | 2012 | 143 | ||
Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients Journal:American Journal of Hematology | 2009 | |||
Variation and heritability of Hb F and F-cells among β-thalassemia heterozygotes in Hong Kong Journal:American Journal of Hematology | 2008 |