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8. Association of variants at BCL11A and HBS1L-MYB with hemoglobin F and hospitalization rates among sickle cell patients in Cameroon. Wonkam A; Ngo Bitoungui VJ; Vorster AA; Ramesar R; Cooper RS; Tayo B; Lettre G; Ngogang J PLoS One; 2014; 9(3):e92506. PubMed ID: 24667352 [TBL] [Abstract][Full Text] [Related]
9. Genetic variants associated with fetal hemoglobin levels show the diverse ethnic origin in Colombian patients with sickle cell anemia. Fong C; Menzel S; Lizarralde MA; Barreto G Biomedica; 2015; 35(3):437-43. PubMed ID: 26849705 [TBL] [Abstract][Full Text] [Related]
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15. SAR1a promoter polymorphisms are not associated with fetal hemoglobin in patients with sickle cell disease from Cameroon. Pule GD; Bitoungui VJN; Chemegni BC; Kengne AP; Wonkam A BMC Res Notes; 2017 May; 10(1):183. PubMed ID: 28499394 [TBL] [Abstract][Full Text] [Related]
16. Original Research: A case-control genome-wide association study identifies genetic modifiers of fetal hemoglobin in sickle cell disease. Liu L; Pertsemlidis A; Ding LH; Story MD; Steinberg MH; Sebastiani P; Hoppe C; Ballas SK; Pace BS Exp Biol Med (Maywood); 2016 Apr; 241(7):706-18. PubMed ID: 27022141 [TBL] [Abstract][Full Text] [Related]
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19. Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans. Bae HT; Baldwin CT; Sebastiani P; Telen MJ; Ashley-Koch A; Garrett M; Hooper WC; Bean CJ; Debaun MR; Arking DE; Bhatnagar P; Casella JF; Keefer JR; Barron-Casella E; Gordeuk V; Kato GJ; Minniti C; Taylor J; Campbell A; Luchtman-Jones L; Hoppe C; Gladwin MT; Zhang Y; Steinberg MH Blood; 2012 Aug; 120(9):1961-2. PubMed ID: 22936743 [No Abstract] [Full Text] [Related]