SEARCH

SEARCH BY CITATION

References

  • Adekile, A.D. & Huisman, T.H. (1993) Hb F in sickle cell anemia. Experientia, 49, 1627.
  • Adekile, A., Al-Kandari, M., Haider, M., Rajaa, M., D’Souza, M. & Sukumaran, J. (2007) Hemoglobin F concentration as a function of age in Kuwaiti sickle cell disease patients. Med Princ Pract, 16, 286290.
  • Akinsheye, I., Alsultan, A., Solovieff, N., Ngo, D., Baldwin, C.T., Sebastiani, P., Chui, D.H. & Steinberg, M.H. (2011) Fetal hemoglobin in sickle cell anemia. Blood, 118, 1927.
  • Bakioglu, I., Kutlar, A. & Huisman, T.H. (1986) Differences between the levels of G gamma chain in the fetal hemoglobin in two types of hereditary persistence of fetal hemoglobin are linked with a variation in the DNA sequence. Biochemical genetics, 24, 149151.
  • Boyer, S.H., Belding, T.K., Margolet, L. & Noyes, A.N. (1975) Fetal hemoglobin restriction to a few erythrocytes (F cells) in normal human adults. Science, 188, 361363.
  • Charache, S. & Conley, C.L. (1969) Hereditary persistence of fetal hemoglobin. Annals of the New York Academy of Sciences, 165, 3741.
  • Charache, S., Terrin, M.L., Moore, R.D., Dover, G.J., Barton, F.B., Eckert, S.V., McMahon, R.P. & Bonds, D.R. (1995) Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia. New England Journal of Medicine, 332, 13171322.
  • Collins, F.S., Cole, J.L., Lockwood, W.K. & Iannuzzi, M.C. (1987) The deletion in both common types of hereditary persistence of fetal hemoglobin is approximately 105 kilobases. Blood, 70, 17971803.
  • Conley, C.L., Weatherall, D.J., Richardson, S.N., Shepard, M.K. & Charache, S. (1963) Hereditary persistence of fetal hemoglobin: a study of 79 affected persons in 15 Negro families in Baltimore. Blood, 21, 261281.
  • Forget, B.G. (1998) Molecular basis of hereditary persistence of fetal hemoglobin. Annals of the New York Academy of Sciences, 850, 3844.
  • Gibbons, R., Higgs, D.R., Old, J.M., Olivieri, N.F., Thein, S.L. & Wood, W.G. (2001) Hereditary persistence of fetal hemoglobin. In: The Thalassemia Syndromes (ed. by D.J. Weatherall & J.B. Clegg), pp. 450483. Blackwell Science Ltd., Malden, MA.
  • Kutlar, A., Gardiner, M.B., Headlee, M.G., Reese, A.L., Cleek, M.P., Nagle, S., Sukumaran, P.K. & Huisman, T.H. (1984) Heterogeneity in the molecular basis of three types of hereditary persistence of fetal hemoglobin and the relative synthesis of the G gamma and A gamma types of gamma chain. Biochemical genetics, 22, 2135.
  • Marcus, S.J., Kinney, T.R., Schultz, W.H., O’Branski, E.E. & Ware, R.E. (1997) Quantitative analysis of erythrocytes containing fetal hemoglobin (F cells) in children with sickle cell disease. American Journal of Hematology, 54, 4046.
  • Padmos, M.A., Roberts, G.T., Sackey, K., Kulozik, A., Bail, S., Morris, J.S., Serjeant, B.E. & Serjeant, G.R. (1991) Two different forms of homozygous sickle cell disease occur in Saudi Arabia. British Journal of Haematology, 79, 9398.
  • Poillon, W.N., Kim, B.C., Rodgers, G.P., Noguchi, C.T. & Schechter, A.N. (1993) Sparing effect of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin S at physiologic ligand saturations. Proceedings of the National Academy of Sciences of the United States of America, 90, 50395043.
  • Steinberg, M.H., Hsu, H., Nagel, R.L., Milner, P.F., Adams, J.G., Benjamin, L., Fryd, S., Gillette, P., Gilman, J., Josifovska, O., Hellman-Erlingsson, S., Safaya, S., Huey, L. & Rieder, R.F. (1995) Gender and haplotype effects upon hematological manifestations of adult sickle cell anemia. American Journal of Hematology, 48, 175181.
  • Thein, S.L. & Wood, W.G. (2009) The molecular basis of β thalassemia, δ-β thalassemia, and hereditary persistence of fetal hemoglobin. In: Disorders of Hemoglobin (ed. by M.H. Steinberg, B.G. Forget, D.R. Higgs & D.J. Weatherall). pp. 341345. Cambridge University Press, New York.
  • Wood, W.G., Stamatoyannopoulos, G., Lim, G. & Nute, P.E. (1975) F-cells in the adult: normal values and levels in individuals with hereditary and acquired elevations of Hb F. Blood, 46, 671682.