| scholarly article | Q13442814 |
| P50 | author | Paola Sebastiani | Q7132103 |
| Martin H Steinberg | Q37380250 | ||
| Lindsay A. Farrer | Q37380266 | ||
| Heather L Edward | Q58179715 | ||
| P2093 | author name string | S Wang | |
| J J Farrell | |||
| C T Baldwin | |||
| P K Patra | |||
| H Bae | |||
| A K Al-Ali | |||
| H Shappell | |||
| D Ngo | |||
| A Alsultan | |||
| A Alsuliman | |||
| A M Al-Rubaish | |||
| D H K Chui | |||
| F Al-Muhanna | |||
| J N Milton | |||
| V Vathipadiekal | |||
| Z Naserullah | |||
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| P433 | issue | 3 | |
| P921 | main subject | sickle-cell disease | Q185034 |
| P304 | page(s) | 224-230 | |
| P577 | publication date | 2015-01-30 | |
| P1433 | published in | Blood Cells, Molecules and Diseases | Q15758051 |
| P1476 | title | BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia | |
| P478 | volume | 54 |
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| Q36191670 | Association between Variants at BCL11A Erythroid-Specific Enhancer and Fetal Hemoglobin Levels among Sickle Cell Disease Patients in Cameroon: Implications for Future Therapeutic Interventions |
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| Q51080070 | Genetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang β-Thalassemia Intermedia Patients. |
| Q26799214 | Genomic approaches to identifying targets for treating β hemoglobinopathies |
| Q41959356 | Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia |
| Q37107201 | Original Research: A case-control genome-wide association study identifies genetic modifiers of fetal hemoglobin in sickle cell disease |
| Q45874809 | Pharmacological and molecular approaches for the treatment of β-hemoglobin disorders. |
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| Q53174215 | Reduced rate of sickle-related complications in Brazilian patients carrying HbF-promoting alleles at the BCL11A and HMIP-2 loci. |
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