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3. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies. Traeger-Synodinos J; Papassotiriou I; Metaxotou-Mavrommati A; Vrettou C; Stamoulakatou A; Kanavakis E Blood Cells Mol Dis; 2000 Aug; 26(4):276-84. PubMed ID: 11042028 [TBL] [Abstract][Full Text] [Related]
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7. Association of mild and severely unstable alpha chain variants: the first observation of a compound heterozygote with Hb Setif [alpha94(G1)Asp-->Tyr (alpha2)] and Hb Agrinio [alpha29(B10)Leu-->Pro (alpha2)] in a Greek family. Douna V; Papassotiriou I; Stamoulakatou A; Metaxotou-Mavrommati A; Kanavakis E; Traeger-Synodinos J Hemoglobin; 2008; 32(6):592-5. PubMed ID: 19065338 [TBL] [Abstract][Full Text] [Related]
8. Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H disease. Viprakasit V; Tanphaichitr VS; Veerakul G; Chinchang W; Petrarat S; Pung-Amritt P; Higgs DR Am J Hematol; 2004 Mar; 75(3):157-63. PubMed ID: 14978697 [TBL] [Abstract][Full Text] [Related]
9. Variable and often severe phenotypic expression in patients with the α-thalassemic variant Hb Agrinio [α29(B10)Leu→Pro (α2)]. Traeger-Synodinos J; Douna V; Papassotiriou I; Stamoulakatou A; Ladis V; Siahanidou T; Fylaktou I; Kanavakis E Hemoglobin; 2010; 34(5):430-8. PubMed ID: 20854116 [TBL] [Abstract][Full Text] [Related]
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11. [Alpha 2 codon 30 deletion (deltaGAG) causing non-deletional hemoglobin H disease in Guangxi province]. Chen P; Li SQ; Wu H Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):435-9. PubMed ID: 15476164 [TBL] [Abstract][Full Text] [Related]
12. Molecular and hematologic features of hemoglobin E heterozygotes with different forms of alpha-thalassemia in Thailand. Sanchaisuriya K; Fucharoen G; Sae-ung N; Jetsrisuparb A; Fucharoen S Ann Hematol; 2003 Oct; 82(10):612-6. PubMed ID: 12955472 [TBL] [Abstract][Full Text] [Related]
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17. Multicenter study of the molecular basis of thalassemia intermedia in different ethnic populations. Verma IC; Kleanthous M; Saxena R; Fucharoen S; Winichagoon P; Raizuddin S; Khan SN; Akbari MT; Izadyar M; Kotea N; Old JM; Ioannou PA; Khan B Hemoglobin; 2007; 31(4):439-52. PubMed ID: 17994378 [TBL] [Abstract][Full Text] [Related]
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19. Observation of a rare hemoglobin variant [Hb Lulu island, beta107(G9)Gly-->Asp, GGC-->GAC] co-inherited with a beta+-thalassemia mutation [IVS-I-110 (G-->A)] or in the heterozygous state in a Greek-Albanian family. Papassotiriou I; Stamoulakatou A; Wajcman H; Kister J; Dimisianos G; Lazaropoulou C; Kanavaki I; Vavourakis E; Kattamis A; Kanavakis E; Traeger-Synodinos J Hemoglobin; 2006; 30(4):409-18. PubMed ID: 16987796 [TBL] [Abstract][Full Text] [Related]
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