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22. Analysis of hemoglobin F production in Saudi Arabian families with sickle cell anemia. Miller BA, Salameh M, Ahmed M, Olivieri N, Antognetti G, Orkin SH, Huisman TH, Nathan DG. Blood; 1987 Sep; 70(3):716-20. PubMed ID: 2441778 [Abstract] [Full Text] [Related]
25. Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients. Labie D, Pagnier J, Lapoumeroulie C, Rouabhi F, Dunda-Belkhodja O, Chardin P, Beldjord C, Wajcman H, Fabry ME, Nagel RL. Proc Natl Acad Sci U S A; 1985 Apr; 82(7):2111-4. PubMed ID: 2580306 [Abstract] [Full Text] [Related]
26. The effect of Hb F and alpha-thalassemia on the red cell indices in sickle cell anemia. Milner PF, Garbutt GJ, Nolan-Davis LV, Jonah F, Wilson LB, Wilson JT. Am J Hematol; 1986 Apr; 21(4):383-95. PubMed ID: 2420172 [Abstract] [Full Text] [Related]
27. Flow cytometric method for simultaneous assay of foetal haemoglobin containing red cells, reticulocytes and foetal haemoglobin containing reticulocytes. Mundee Y, Bigelow NC, Davis BH, Porter JB. Clin Lab Haematol; 2001 Jun; 23(3):149-54. PubMed ID: 11553054 [Abstract] [Full Text] [Related]
28. 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]
29. Reference values and hematologic changes from birth to 5 years in patients with sickle cell disease. Cooperative Study of Sickle Cell Disease. Brown AK, Sleeper LA, Miller ST, Pegelow CH, Gill FM, Waclawiw MA. Arch Pediatr Adolesc Med; 1994 Aug 08; 148(8):796-804. PubMed ID: 7519102 [Abstract] [Full Text] [Related]