Absence of hemoglobin A in a double heterozygote for F-thalassemia and hemoglobin S von Stamatoyannopoulos, G, Sofroniadou, C, Akrivakis, A

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Further data from Greece on recombination between the Xg blood group and glucose-6-phosphate dehydrogenase deficiency von Stamatoyannopoulos, G, Sofroniadou, C, Akrivakis, A, Fraser, G R

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BRIEF REPORT: Absence of Hemoglobin A in a Double Heterozygote for F-Thalassemia and Hemoglobin S von STAMATOYANNOPOULOS, C., SOFRONIADOU, C., AKRIVAKIS, A.

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Absence of chemotherapy-induced alopecia with paclitaxel in a case of hypothyroidism: case report von Sofroniadou, S., Kosmas, C., Kourelis, T., Makatsoris, T., Koutras, A., Onienadoum, A., Kalofonos, H. P.

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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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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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Hemoglobin pyrgos alpha2 beta2 83 (EF7) Gly leads to Asp: a new hemoglobin variant in double heterozygosity with hemoglobin S von Tatsis, B, Sofroniadou, K, Stergiopoulos, CI

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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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Hemoglobin pyrgos alpha2 beta2 83 (EF7) Gly leads to Asp: a new hemoglobin variant in double heterozygosity with hemoglobin S von Tatsis, B, Sofroniadou, K, Stergiopoulos, C I

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