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Journal Abstract Search

155 related items for PubMed ID: 17486510

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  • 7. The molecular basis of Hb H disease in Turkey.
    Oner C, Gürgey A, Oner R, Balkan H, Gümrük F, Baysal E, Altay C.
    Hemoglobin; 1997 Jan; 21(1):41-51. PubMed ID: 9028822
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  • 12. A rare thalassemic syndrome caused by interaction of Hb Adana [alpha59(E8)Gly-->Asp] with an alpha+-thalassemia deletion: clinical aspects in two cases.
    Douna V, Papassotiriou I, Garoufi A, Georgouli E, Ladis V, Stamoulakatou A, Metaxotou-Mavrommati A, Kanavakis E, Traeger-Synodinos J.
    Hemoglobin; 2008 Jan; 32(4):361-9. PubMed ID: 18654886
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  • 13. Dominantly Inherited beta-Thalassemia.
    Efremov GD.
    Hemoglobin; 2007 Jan; 31(2):193-207. PubMed ID: 17486503
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  • 15. Nondeletional Hb Queens Park [α32(B13)Met→Lys]/Hb H (β4) disease.
    Sroymora S, Jindadamrongwech S, Butthep P, Chuncharunee S.
    Hemoglobin; 2012 Jan; 36(3):293-8. PubMed ID: 22384838
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  • 17. Prenatal diagnosis of sickle cell anemia and beta-thalassemia in southern Turkey.
    Cürük MA, Zeren F, Genç A, Ozavci-Aygün S, Kilinç Y, Aksoy K.
    Hemoglobin; 2008 Jan; 32(6):525-30. PubMed ID: 19065329
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