Interaction of heterocellular hereditary persistence of foetal haemoglobin with β thalassaemia and sickle cell anaemia

The Thalassæmia Syndromes.

The Medical Journal of Australia · 1973 · 812 citations

Irreversibly sickled erythrocytes: a consequence of the heterogeneous distribution of hemoglobin types in sickle-cell anemia

John F. Bertles, Paul Milner · Journal of Clinical Investigation · 1968 · 267 citations · Full text

Medicine, Biochemistry, Hematology +17

F-cells in the adult: normal values and levels in individuals with hereditary and acquired elevations of Hb F

W. G. Wood, G Stamatoyannopoulos, G. Lim et al. · Blood · 1975 · 249 citations · Full text

Medicine, Cell Biology, Hematology +5

Fetal Hemoglobin Restriction to a Few Erythrocytes (F Cells) in Normal Human Adults

Samuel H. Boyer, Thomas K. Belding, Louise Margolet et al. · Science · 1975 · 244 citations

Medicine, Hematology, Cell Physiology +8

A new form of hereditary persistence of fetal hemoglobin in blacks and its association with sickle cell trait

G. Stamatoyannopoulos, WG Wood, T Papayannopoulou et al. · Blood · 1975 · 102 citations · Full text

Life Sciences, Genetics, Hematology +10