SEARCH

SEARCH BY CITATION

References

  • Bernini, L.F. & Harteveld, C.L. (1998) Alpha-thalassaemia. Bailliéres Clin Haematol, 11, 5390.
  • Blackwell, R.Q., Boon, W.H., Liu, C.S. & Weng, M.I. (1972) Hemoglobin J Singapore: alpha 78 Asn--Asp; alpha 79 Ala--Gly. Biochimica et Biophysica Acta, 278, 482490.
  • Fichera, M., Spalletta, A., Fiorenza, F., Lombardo, T., Schilirò, G., Tamouza, R., Lapoumeroulie, C., Labie, D. & Ragusa, A. (1997) Molecular basis of thalassemia in Sicily. Human Genetics, 99, 381386.
  • Foglietta, E., Deidda, G., Graziani, B., Modiano, G. & Bianco, I. (1996) Detection of α-globin gene disorders by a simple PCR methodology. Haematologica, 81, 387396.
  • Giambona, A., Passarello, C., Ruggeri, G., Renda, D., Teresi, P., Anzà, M. & Maggio, A. (2006) Analysis of delta-globin gene alleles in the Sicilian population: identification of five new mutations. Haematologica, 91, 16811684.
  • Guida, V., Colorino, A., Fichera, M., Lombardo, T., Rigoli, L. & Dalla piccola, B. (2006) Hematologic and molecular characterizaion of a Sicilian cohort of alpha-thalassemia carriers. Haematologica, 91, 409410.
  • Harkness, M., Harkness, D.R., Kutlar, F., Kutlar, A., Wilson, J.B., Webber, B.B., Codrington, J.F. & Huisman, T.H. (1990) Hb Sun Prairie or alpha(2)130(H13)Ala----Pro beta 2, a new unstable variant occurring in low quantities. Hemoglobin, 14, 491497.
  • Ho, P.J., Rochette, J., Rees, D.C., Fisher, C.A., Huehns, E.R., Will, A.M. & Thein, S.L. (1996) Hb Sun Prairie: diagnostic pitfalls in thalassemic hemoglobinophathies. Hemoglobin, 20, 103112.
  • Husman, T.H.J. & Jonxis, J.H.P. (1977) Techiniques of Identification. Clinical and Biochemical Analysis. Vol. 6, Marcel Dekker. Inc., New York.
  • Miller, S.A., Dyles, D.D. & Polesky, H.F. (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acid Research, 16, 1215.
  • Papassotiriou, I., Traeger-Synodinos, J., Vlachou, C., Karagiorga, M., Metaxotou, A., Kanavakis, E. & Stamoulakatou, A. (1999) Rapid and accurate quantitation of hemoglobins Bart’s and HbH using weak cation-exchange high pressure liquid chromatography: correlation with the alpha thalassemia genotype. Hemoglobin, 23, 203211.
  • Sarkar, A.A., Mukhopadhyay, C., Chandra, S., Banerjee, S., Das, M.K. & Dasgupta, U.M. (2005) Co-inheritance of Hb Sun Prairie mutation with point mutation at 5′-UTR in the eastern Indian population. British Journal of Haematology, 129, 282286.
  • Ventruto, V., Derosa, L., Bianchi, P., Ricchi, L. & Quattrini, N. (1964) Description of a new slow hemoglobin in a Casertian family (Hb Caserta). Il Progresso Medico, 20, 157162.
  • Weatherall, D.J., Clegg, J.B., Higgs, D.R. & Wood, W.H. (2001) The hemoglobinopathies. In: The Metabolic and Molecular Bases of Inherited Disease (ed. by C.R.Scriver), pp. 45714636. McGraw-Hill, New York.
  • Wenning, M.R., Silva, N.M., Jorge, S.B., Kimura, E.M., Costa, F.F., Torsoni, F., Ogo, S.H. & Sonati, M.F. (2000) Hb Campinas [alpha26(B7)Ala -->Val]: a novel, electrophoretically silent, variant. Hemoglobin, 24, 143148.
  • Zeng, Y.T., Huang, S.Z., Zhou, X.D., Qiu, X.K., Dong, Q.Y., Li, M.Y. & Bai, J.H. (1982) Hb Shenyang (alpha 26 (B7) Ala replaced by Glu): a new unstable variant found in China. Hemoglobin, 6, 625628.