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8. The Senegal DNA haplotype is associated with the amelioration of anemia in African-American sickle cell anemia patients. Nagel RL, Erlingsson S, Fabry ME, Croizat H, Susuka SM, Lachman H, Sutton M, Driscoll C, Bouhassira E, Billett HH. Blood; 1991 Mar 15; 77(6):1371-5. PubMed ID: 2001460 [Abstract] [Full Text] [Related]
12. The hematologic characteristics of sickle cell anemia bearing the Bantu haplotype: the relationship between G gamma and HbF level. Nagel RL, Rao SK, Dunda-Belkhodja O, Connolly MM, Fabry ME, Georges A, Krishnamoorthy R, Labie D. Blood; 1987 Apr 15; 69(4):1026-30. PubMed ID: 2435339 [Abstract] [Full Text] [Related]
14. Beta-globin gene cluster haplotypes and HbF levels are not the only modulators of sickle cell disease in Lebanon. Inati A, Taher A, Bou Alawi W, Koussa S, Kaspar H, Shbaklo H, Zalloua PA. Eur J Haematol; 2003 Feb 15; 70(2):79-83. PubMed ID: 12581188 [Abstract] [Full Text] [Related]
16. Localisation of cis regulatory elements at the beta-globin locus: analysis of hybrid haplotype chromosomes. Ofori-Acquah SF, Lalloz MR, Layton DM. Biochem Biophys Res Commun; 1999 Jan 08; 254(1):181-7. PubMed ID: 9920754 [Abstract] [Full Text] [Related]
17. The influence of fetal hemoglobin on the clinical expression of sickle cell anemia. Powars DR, Chan L, Schroeder WA. Ann N Y Acad Sci; 1989 Jan 08; 565():262-78. PubMed ID: 2476064 [Abstract] [Full Text] [Related]