| Issue Date | Title | Author(s) |
| 1985 | (Aγδβ)ο-Thalassaemia in Blacks is due to a deletion of 34 kbp of DNA | Henthorn, P. S.; Smithies, O.; Nakatsuji, T.; Felice, Alex; Gardiner, M. B.; Reese, A. L.; Huisman, T. H. J. |
| 1984 | Deletions and duplications of α or ζ globin genes in children with sickle cell anemia | Felice, Alex; McKie, Virgil C.; McKie, Kathleen M.; Huisman, T. H. J. |
| 1984 | The effect of deletions and reduplications on the expression of human α and ζ globin genes | Felice, Alex; McKie, Kathleen M.; McKie, Virgil C.; Huisman, T. H. J. |
| 1981 | Hb G-Philadelphia in asociation with Hb S and α-Thalassemia-2 | Felice, Alex; Ozdonmez, R.; Headlee, M. E.; Huisman, T. H. J. |
| 1978 | Hb P Nilotic – β0 thalassemia : mutation of a human hemoglobin regulatory gene? | Felice, Alex; Abu-sin, Ahmed; Huisman, T. H. J. |
| 1979 | Hb P-Nilotic in association with βo-thalassemia : cis-mutation of a hemoglobin βa chain regulatory determinant? | Abu-sin, Ahmed; Felice, Alex; Gravely, M. E.; Wilson, J. B.; Reese, A. L.; Lam, H.; Miller, A.; Huisman, T. H. J. |
| 1989 | Hb Valletta [α2β287(F3)Thr→Pro] and Hb F-Malta-I [α2Gγ2117 (619)His→Arg] are in linkage in the Maltese population. | Felice, Alex; Grech, J. L.; Bannister, W. H.; Kutlar, F.; Kutlar, A.; Wilson, J. B.; Webber, B. B.; Hu, H.; Huisman, T. H. J. |
| 1983 | Hemoglobin production on stimulation of K562 human pluripotent leukemia cells | Felice, Alex; Mayson, S. M.; Reese, A. L.; Huisman, T. H. J. |
| 1980 | In vitro synthesis of hemoglobin in BFU-e derived colonies of persons with an α or a β-Thalassemia | Felice, Alex; Altay, C. A.; Reese, A. L.; Webber, B.; Huisman, T. H. J. |
| 1983 | The occurrence of α chain gene deletions and triplications among pediatric Hb S homozygotes | Felice, Alex; Cleek, M. P.; Lewis, J. P.; McKie, Virgil C.; McKie, Kathleen M.; Harris, H. F.; Huisman, T. H. J. |
| 1978 | Sickle Cell Amenia in association with α-thalassemia-2 : biosynthetic and hematological studies | Felice, Alex; Huisman, T. H. J. |
| 1978 | Variability in the interaction of β-thalassemia with the α-chain variants Hb G-Philadelphia and Hb Rampa | Huisman, T. H. J.; Gravely, M. E.; Henson, J.; Felice, Alex; Wilson, J. B.; Abraham, E. C.; Vella, Frank; Little, M. W. |
| 1978 | δβ-Thalassemia in a Mexican family : clinical differences among homozygotes | Ruiz Reyes, Guillermo; Pina-Camara, Arturo; Felice, Alex; Gravely, M. E.; Huisman, T. H. J. |
