Red cell enzymes in trisomy 21 von Pantelakis, S N, Karaklis, A G, Alexiou, D, Vardas, E, Valaes, T

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Concordance of a point mutation 5' to the Aγ-globin gene with Aγβ+ hereditary persistence of fetal hemoglobin in greeks von WABER, P. G, BENDER, M. A, GELINAS, R. E, KATTANIS, C, KARAKLIS, A, SOFRONIADOU, K, STAMATOYANNOPOULOS, G, COLLINS, F. S, FORGET, B. G, KAZAZIAN, H. H. JR

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Hemoglobin “Pylos”: Study of a Hemoglobinopathy Resembling Thalassemia in the Heterozygous, Homozygous and Double Heterozygous State von Fessas, Phaedon, Stamatoyannopoulos, Georges, Karaklis, Aris

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Concordance of a point mutation 5' to the A gamma-globin gene with A gamma beta + hereditary persistence of fetal hemoglobin in Greeks von Waber, P G, Bender, M A, Gelinas, R E, Kattamis, C, Karaklis, A, Sofroniadou, K, Stamatoyannopoulos, G, Collins, F S, Forget, B G, Kazazian, Jr, H H

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Concordance of a Point Mutation 5’ to the Aγ-Globin Gene With Aγß+Hereditary Persistence of Fetal Hemoglobin in Greeks von Waber, Pamela G., Bender, Michael A., Gelinas, Richard E., Kattamis, Christos, Karaklis, Aris, Sofroniadou, Koula, Stamatoyannopoulos, George, Collins, Francis S., Forget, Bernard G., Kazazian, Haig H.

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Concordance of a point mutation 5' to the A gamma-globin gene with A gamma beta + hereditary persistence of fetal hemoglobin in Greeks von Waber, PG, Bender, MA, Gelinas, RE, Kattamis, C, Karaklis, A, Sofroniadou, K, Stamatoyannopoulos, G, Collins, FS, Forget, BG, Kazazian, HH Jr

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Three inherited red-cell abnormalities in a district of Greece. Thalassaemia, sickling, and glucose-6-phosphate-dehydrogenase deficiency von CHOREMIS, C, FESSAS, P, KATTAMIS, C, STAMATOYANNOPOULOS, G, ZANNOS-MARIOLEA, L, KARAKLIS, A, BELIOS, G

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THREE INHERITED RED-CELL ABNORMALITIES IN A DISTRICT OF GREECE: Thalassæmia, Sickling, and Glucose-6-phosphate-dehydrogenase Deficiency von Choremis, C., Fessas, PH, Kattamis, C., Stamatoyannopoulos, G., Zannos-Mariolea, L., Karaklis, A., Belios, G.

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