GENETIC BASIS OF THE THALASSAEMIA DISEASES

[1] BINGLE JP, 1958, BRIT MED J, P1389

[2] CEPPELLINI R, 1958, HEMOGLOBIN

[3] CEPPELLINI R, 1958, 7 C INT SOC HAEM ROM, P47

[4] MULTIPLE INHERITED ERYTHROCYTE ABNORMALITIES IN AN AMERICAN NEGRO FAMILY - HEREDITARY SPHEROCYTOSIS, SICKLING AND THALASSEMIA [J]. BLOOD, 1959, 14 (07) : 816 - 827

[5] FESSAS P, 1959, ABNORMAL HAEMOGLOBIN, P153

[6] THE ARRANGEMENT OF DNA IN THE CHROMOSOME [J]. COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1958, 23 : 13 - 18

[7] THE DIAGNOSIS OF THALASSEMIA TRAIT BY STARCH BLOCK ELECTROPHORESIS OF THE HEMOGLOBIN [J]. BLOOD, 1958, 13 (01) : 61 - 69

[8] GERALD PS, 1958, HEMOGLOBIN

[9] IDENTITY OF THE ALPHA-CHAINS OF ADULT AND FOETAL HUMAN HAEMOGLOBINS [J]. NATURE, 1959, 183 (4672) : 1373 - 1375

[10] SPECIFIC CHEMICAL DIFFERENCE BETWEEN THE GLOBINS OF NORMAL HUMAN AND SICKLE-CELL ANAEMIA HAEMOGLOBIN [J]. NATURE, 1956, 178 (4537) : 792 - 794

[1] BINGLE JP, 1958, BRIT MED J, P1389

[2] CEPPELLINI R, 1958, HEMOGLOBIN

[3] CEPPELLINI R, 1958, 7 C INT SOC HAEM ROM, P47

[4] MULTIPLE INHERITED ERYTHROCYTE ABNORMALITIES IN AN AMERICAN NEGRO FAMILY - HEREDITARY SPHEROCYTOSIS, SICKLING AND THALASSEMIA [J]. BLOOD, 1959, 14 (07) : 816 - 827

[5] FESSAS P, 1959, ABNORMAL HAEMOGLOBIN, P153

[6] THE ARRANGEMENT OF DNA IN THE CHROMOSOME [J]. COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1958, 23 : 13 - 18

[7] THE DIAGNOSIS OF THALASSEMIA TRAIT BY STARCH BLOCK ELECTROPHORESIS OF THE HEMOGLOBIN [J]. BLOOD, 1958, 13 (01) : 61 - 69

[8] GERALD PS, 1958, HEMOGLOBIN

[9] IDENTITY OF THE ALPHA-CHAINS OF ADULT AND FOETAL HUMAN HAEMOGLOBINS [J]. NATURE, 1959, 183 (4672) : 1373 - 1375

[10] SPECIFIC CHEMICAL DIFFERENCE BETWEEN THE GLOBINS OF NORMAL HUMAN AND SICKLE-CELL ANAEMIA HAEMOGLOBIN [J]. NATURE, 1956, 178 (4537) : 792 - 794