Tetralogy of Fallot with hypoxemia in a patient with beta thalassemia intermedia.

[1]  D. Fitzsimons,et al.  Congenital Disorders of Erythropoiesis , 1976 .

[2]  G. Stamatoyannopoulos,et al.  F-cells in the adult: normal values and levels in individuals with hereditary and acquired elevations of Hb F. , 1975, Blood.

[3]  J. Clegg,et al.  Imbalanced globin chain synthesis in heterozygous beta-thalassemic bone marrow. , 1975, Proceedings of the National Academy of Sciences of the United States of America.

[4]  S. Boyer,et al.  Fetal hemoglobin restriction to a few erythrocytes (F cells) in normal human adults. , 1975, Science.

[5]  B. Ramot,et al.  Globin synthesis in iron-deficiency anemia. , 1974, Blood.

[6]  W. Anderson,et al.  Hemoglobin messenger RNA from human bone marrow. Isolation and translation in homozygous and heterozygous beta-thalassemia. , 1973, The Journal of clinical investigation.

[7]  R. Loewenson,et al.  Body growth in Cooley's anemia (homozygous beta-thalassemia) with a correlative study as to other aspects of the illness in 138 cases. , 1972, Pediatrics.

[8]  R. Gunn,et al.  Potassium permeability in -thalassemia minor red blood cells. , 1972, The Journal of clinical investigation.

[9]  G. Cividalli,et al.  Increased permeability of erythrocyte membrane in thalassemia. , 1971, Blood.

[10]  J. Adamson,et al.  FERROKINETICS IN MAN , 1970, Medicine.

[11]  E. Schwartz The silent carrier of beta thalassemia. , 1969, The New England journal of medicine.

[12]  J. Adamson,et al.  The erythropoietin-hematocrit relationship in normal and polycythemic man: implications of marrow regulation. , 1968, Blood.

[13]  R. Gunn,et al.  Thalassemia: the consequences of unbalanced hemoglobin synthesis. , 1966, The American journal of medicine.

[14]  J. Clegg,et al.  Abnormal human haemoglobins , 1966 .

[15]  R. Weed,et al.  Metabolic dependence of the critical hemolytic volume of human erythrocytes: relationship to osmotic fragility and autohemolysis in hereditary spherocytosis and normal red cells. , 1966, The Journal of clinical investigation.

[16]  J. Macdonald THE MOLECULAR DEFECT IN THALASSEMIA. , 1964, Nutrition reviews.

[17]  J. Blomfield,et al.  Alkali‐Resistant Haemoglobin Content of Blood in Congenital Heart Disease , 1963, British journal of haematology.

[18]  Moseley Je The thalassemias: variants and roentgen bone changes. , 1962 .

[19]  R. Sanger,et al.  Blood Groups in Man , 1959 .

[20]  A. Chernoff,et al.  Determinations of fetal hemoglobin in whole blood, using a modified alkali denaturation test. , 1958, American journal of clinical pathology.

[21]  C. Smith,et al.  Fetal and adult hemoglobins in hemolytic disease of the newborn. , 1954, A.M.A. American journal of diseases of children.

[22]  B. Forget,et al.  The molecular genetics of the thalassemia syndromes. , 1975, Progress in hematology.

[23]  W. Anderson,et al.  Hemoglobin Messenger RNA from Human Bone Marrow , 1973 .

[24]  S. Yang From cardiac catheterization data to hemodynamic parameters , 1972 .

[25]  R. Karp,et al.  The tetralogy of Fallot from a surgical viewpoint , 1970 .

[26]  R. Gunn,et al.  Influence of hemoglobin precipitation on erythrocyte metabolism in alpha and beta thalassemia. , 1969, The Journal of clinical investigation.

[27]  M. Rörth,et al.  An enzymatic assay of 2,3-diphosphoglycerate in blood. , 1969, Scandinavian journal of clinical and laboratory investigation.