Sickle cell--betao thalassemia variant with high hemoglobin F and mild clinical course.

[1]  J. Shaeffer,et al.  Patterns of hemoglobin assembly in reticulocytes of sickle cell trait individuals. , 1975, The Journal of biological chemistry.

[2]  Kazazian Hh Regulation of fetal hemoglobin production , 1974 .

[3]  A. Bank,et al.  Balanced globin chain synthesis in hereditary persistence of fetal hemoglobin. , 1974, The Journal of clinical investigation.

[4]  J. Shaeffer,et al.  Unbalanced globin chain synthesis in reticulocytes of sickle cell trait individuals with low concentrations of hemoglobin S. , 1974, Biochemical and biophysical research communications.

[5]  J. White,et al.  The Synthesis of Globin Peptide Chains in Sickle‐Cell Disease , 1974, British journal of haematology.

[6]  J. Shaeffer Structure and synthesis of the unstable hemoglobin Sabin (alpha 2 beta 2--91 Leu leads to pro). , 1973, The Journal of biological chemistry.

[7]  M. Farace,et al.  Changes in globin synthesis with erythroid cell maturation in sickle thalassemia. , 1973, Blood.

[8]  F. Gill,et al.  Synthesis of globin chains in sickle -thalassemia. , 1973, The Journal of clinical investigation.

[9]  P. Milner,et al.  The clinical features of sickle-cell- thalassaemia in Jamaica. , 1973, British journal of haematology.

[10]  H. Pearson HEMOGLOBIN S‐THALASSEMIA SYNDROME IN NEGRO CHILDREN 1 , 1969, Annals of the New York Academy of Sciences.

[11]  J. Clegg,et al.  The Pattern of Disordered Haemoglobin Synthesis in Homozygous and Heterozygous β‐Thalassaemia * , 1969, British journal of haematology.

[12]  J. B. Clegg,et al.  The thalassaemia syndromes , 1965 .

[13]  D. Weatherall Biochemical Phenotypes of Thalassemia in the American Negro Population * , 1964, Annals of the New York Academy of Sciences.