MICRODREPANOCYTIC DISEASE IN GREECE

[1] CHOREMIS C, 1952, SCHWEIZ MED WSCHR, V82, P709

[2] CHOREMIS C, 1953, LANCET 1031, P11

[3] DELIJANNIS G, 1954, ELLINIKI IATRIKI, V23

[4] GIRAUD P, 1955, Arch Fr Pediatr, V12, P214

[5] THE ABNORMAL HUMAN HEMOGLOBINS [J]. MEDICINE, 1956, 35 (02) : 121 - 159

[6] LAHEY ME, 1954, AMA AM J DIS CHILD, V88, P649

[7] 2 CASES OF SICKLE CELL DISEASE PRESUMABLY DUE TO THE COMBINATION OF THE GENES FOR THALASSEMIA AND SICKLE CELL HEMOGLOBIN [J]. BLOOD, 1953, 8 (05) : 434 - 443

[8] THE OCCURRENCE IN A FAMILY OF SICILIAN ANCESTRY OF THE TRAITS FOR BOTH SICKLING AND THALASSEMIA [J]. BLOOD, 1950, 5 (10) : 887 - 897

[9] GENETIC ASPECTS OF SICKLE CELL ANEMIA AND MICRODREPANOCYTIC DISEASE [J]. BLOOD, 1952, 7 (04) : 429 - 435

[10] NEW DATA ON MICRODREPANOCYTIC DISEASE [J]. BLOOD, 1955, 10 (06) : 623 - 632

[1] CHOREMIS C, 1952, SCHWEIZ MED WSCHR, V82, P709

[2] CHOREMIS C, 1953, LANCET 1031, P11

[3] DELIJANNIS G, 1954, ELLINIKI IATRIKI, V23

[4] GIRAUD P, 1955, Arch Fr Pediatr, V12, P214

[5] THE ABNORMAL HUMAN HEMOGLOBINS [J]. MEDICINE, 1956, 35 (02) : 121 - 159

[6] LAHEY ME, 1954, AMA AM J DIS CHILD, V88, P649

[7] 2 CASES OF SICKLE CELL DISEASE PRESUMABLY DUE TO THE COMBINATION OF THE GENES FOR THALASSEMIA AND SICKLE CELL HEMOGLOBIN [J]. BLOOD, 1953, 8 (05) : 434 - 443

[8] THE OCCURRENCE IN A FAMILY OF SICILIAN ANCESTRY OF THE TRAITS FOR BOTH SICKLING AND THALASSEMIA [J]. BLOOD, 1950, 5 (10) : 887 - 897

[9] GENETIC ASPECTS OF SICKLE CELL ANEMIA AND MICRODREPANOCYTIC DISEASE [J]. BLOOD, 1952, 7 (04) : 429 - 435

[10] NEW DATA ON MICRODREPANOCYTIC DISEASE [J]. BLOOD, 1955, 10 (06) : 623 - 632